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Enforcement Report - Week of October 24, 2012

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Biologics Devices Drugs Food / Cosmetics Veterinary

Class I Devices Event

Event ID	62879
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	03-Aug-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Ethicon Endo-Surgery Inc
City	Cincinnati
State	OH
Country	US
Distribution Pattern	Worldwide Distribution - US (nationwide) in the states of: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of: ARGENTINA, AUSTRALIA, BAHRAIN, BELGIUM, BRAZIL, CHILE, CHINA, COLOMBIA, COSTA RICA, CYPRUS, DOMINICAN REPUBLIC, ECUADOR, EGYPT, EL SALVADOR, GREECE, GUATEMALA, HONG KONG, INDIA, INDONESIA, ISRAEL, ITALY, JAPAN, JORDAN, REPUBLIC OF KOREA, KUWAIT, LEBANON, MALAYSIA, MEXICO, NEPAL, NICARAGUA, PAKISTAN, PANAMA, PARAGUAY, PERU, PHILIPPINES, PUERTO RICO, RUSSIA, SAUDI ARABIA, SINGAPORE, SLOVENIA, SOUTH AFRICA, TAIWAN, THAILAND, TURKEY, UNITED ARAB EMIRATES, URUGUAY, VENEZUELA, VIETNAM, and YEMEN. There was one Canadian consignee and 43 U.S. Government consignees.

Associated Products

Product Description	Hemorrhoidal Circular Stapler and Accessories 33mm Product Usage: The PROXIMATE HCS Hemorrhoidal Circular Staplers, (PPH01 and PPH03), and accessories have application for general surgical treatment of anorectal wall defects by means of transanal stapling and resection of mucosal and musculomucosal tissue. The TRANSTARTM CIRCULAR STAPLER, (STR10), and accessories have application for general surgical treatment of anorectal wall defects by means of transanal stapling and resection of mucosal and musculomucosal tissue.
Code Info	PPH01: 68 lots; 19,030 pieces; Expiration date April 2016 -June 2017; PPH03: 494 lots; 144,963 pieces; Expiration date March 2016 - June 2017; STR10: 3 lots; 432 pieces; Expiration date Sept 2016 - Oct 2016
Classification	Class I
Reason for Recall	Ethicon Endo-Surgery initiated this voluntary global recall for specific production lots of PROXIMATE® PPH Hemorrhoidal Circular Stapler and Accessories 33mm (PPH01 and PPH03) and Transtar® Circular Stapler Procedure Set (STR10) due to difficulty firing the device which may result in incomplete firing stroke that may result in an incomplete staple formation.
Product Quantity	157,881 devices
Recall Number	Z-0057-2013

Class I Food/Cosmetics Event

Event ID	63032
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	25-Aug-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Splendid Products
City	Burlingame
State	CA
Country	US
Distribution Pattern	Nationwide distribution.

Associated Products

Product Description	Daniella Mangoes May be identified by Daniella sticker with a PLU code of 3114, 4051, 4311, 4584 or 4959.
Code Info	All fruit had identifying stickers with label "Daniella" and one of the following PLU numbers: 3114, 4051, 4311, 4584 or 4959.
Classification	Class I
Reason for Recall	Firm is recalling certain lots of Daniella brand mangoes because they may be contaminated with Salmonella. Mangoes have been linked to a number of recent cases of salmonellosis in Canada, and may be linked to cases in California and perhaps other states
Product Quantity	~1,200,000 cases shipped to US.
Recall Number	F-2395-2012

Class I Food/Cosmetics Event

Event ID	63101
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	30-Aug-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	Harry and David Operations, Inc.
City	Medford
State	OR
Country	US
Distribution Pattern	Internet sales to 44 states and the District of Columbia

Associated Products

Product Description	Cushman's Fruit and Flower Basket
Code Info	205 through 242 printed on the shipping container. The format of the lot code is ###2M, with ### representing the numbers 205 through 242.
Classification	Class I
Reason for Recall	Daniella brand mangoes recalled due to potential contamination with Salmonella. Firm used mangoes in their fruit baskets.
Product Quantity	739 total for recall
Recall Number	F-0144-2013

Product Description	Cushman's New All Fruit Basket
Code Info	205 through 242 printed on the shipping container. The format of the lot code is ###2M, with ### representing the numbers 205 through 242.
Classification	Class I
Reason for Recall	Daniella brand mangoes recalled due to potential contamination with Salmonella. Firm used mangoes in their fruit baskets.
Product Quantity
Recall Number	F-0145-2013

Product Description	Harry and David Fresh Fruit Gift Basket and Fresh Fruit Gift Basket Deluxe
Code Info	205 through 242 printed on the shipping container. The format of the lot code is ###2M, with ### representing the numbers 205 through 242.
Classification	Class I
Reason for Recall	Daniella brand mangoes recalled due to potential contamination with Salmonella. Firm used mangoes in their fruit baskets.
Product Quantity
Recall Number	F-0146-2013

Product Description	Harry and David and Cushman's Original Gift Baskets
Code Info	205 through 242 printed on the shipping container. The format of the lot code is ###2M, with ### representing the numbers 205 through 242.
Classification	Class I
Reason for Recall	Daniella brand mangoes recalled due to potential contamination with Salmonella. Firm used mangoes in their fruit baskets.
Product Quantity
Recall Number	F-0147-2013

Class I Food/Cosmetics Event

Event ID	63149
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	16-Aug-12
Initial Firm Notification of Consignee or Public	E-Mail

Recalling Firm	J & J Snack Foods Corporation
City	Pennsauken
State	NJ
Country	US
Distribution Pattern	Nationwide

Associated Products

Product Description	Luigi's Real Italian Ice Birthday Cake 6 FL OZ cups Net Wt 36 FL OZ (1.06 L) upc 73321-04418 J & J Snack Foods Corp. Pennsauken, NJ 08109 USA at Plant #42-2479 www.luigis.com
Code Info	Best By: NOV 23 2013 FEB 15 2014 FEB 16 2014 FEB 17 2014 MAY 14 2014 MAY 15 2014 JUN 10 2014 JUN 11 2014
Classification	Class I
Reason for Recall	Luigi's Real Italian Ice Birthday Cake Flavor is mislabeled as "Dairy-Free".
Product Quantity	25,948 CASES
Recall Number	F-0079-2013

Class I Food/Cosmetics Event

Event ID	63184
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	11-Sep-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Whole Foods Market
City	Austin
State	TX
Country	US
Distribution Pattern	Nationwide to 21 states

Associated Products

Product Description	Frescolina and Mitica brand Ricotta Salata cheeses were cut into wedges, packaged in clear plastic wrap and sold with a Whole Foods Market scale label using PLU 293427 and PLU 294413, respectively. All "sell by" dates through Oct. 2 are affected.
Code Info	Frescolina Ricotta Salata PLU 293427. Mitica Ricotta Salata PLU 294413. All with Sell by dates Oct 2, 2012.
Classification	Class I
Reason for Recall	Whole Foods Market announces that it is recalling ricotta salata sold in 21 states and Washington, D.C. that came from its supplier Forever Cheese Inc. of Long Island City, NY. Forever Cheese recalled this cheese product because it may be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Product Quantity	Approximately 2500 lbs
Recall Number	F-0110-2013

Class I Food/Cosmetics Event

Event ID	63193
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	15-Sep-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	Caito Foods Service, Inc.
City	Indianapolis
State	IN
Country	US
Distribution Pattern	4 Distributors in WI, IN, IL, CA with further nationwide distribution to retail stores

Associated Products

Product Description	Nice, Fruit Mango, Product of Mexico, single, 6 ct; UPC 0.4902252988.5
Code Info	Item Number 381030, Best By 8/04/12 -09/14/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella,Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	497
Recall Number	F-0127-2013

Product Description	deLISH, fresh, Pineapple, mango, & cantaloupe spears ( 5 oz), UPC 0.49022-53701.9 and tropical medley, (10 oz), UPC 0.49022-53699.9. Prepared for Walgreen, Inc. Deerfield, IL 60015. Ingredients: Cantaloupe, Mango, Pineapple, Packed in its Own Juice, Grown In USA, Mexico, Costa Rica
Code Info	Spears:Item 383138; Best By 8/04/12 -09/14/12 Medey :item 383137; Best By 8/04/12 -09/14/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	2633 cases medley, 2137 cases spears
Recall Number	F-0128-2013

Product Description	DeLish, Garden Highway and Generic brands of Fruit Burst, Ingredients: cantaloupe, pineapple, honeydew, watermelon, grapes, strawberries, mango, blueberries packed in its Own Juice; deLISH (Brand), fresh, , Prepared for Walgreen, Inc. Deerfield, IL 60015, 10oz. Generic (Brand ) Sold at Wal-Mart Stores: Fruit Burst: 16 oz (1 lb) and 48 oz( 3 lbs); Garden Highway Brand 10 oz. , 16 oz (1 lb); 32 oz (2 lb)
Code Info	DeLish Item 383096; 10-oz; UPC 0.49022-55862.5; Generic items, sold at Walmart, 383097,383095; UPC 8.26766-22545.3 and 8.26766-25552.8; Garden Highway, Item 383102, 383836, 383837; UPC 8.26766-24106.4, 8.26766 -24107, 8.26766-24109.5; Best By 08/04/2012- 9/16/2012
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	all types 16,297 cases
Recall Number	F-0129-2013

Product Description	deLISH, fresh, Mango & Berry Mix, 10oz., UPC 0.49022-63779.5, Prepared for Walgreen, Inc. Deerfield, IL 60015, Ingredients: Mango, strawberries, blueberries packed in its Own Juice.
Code Info	Item 383827; Best By 8/04/2012- 09/16/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	1062 cases
Recall Number	F-0130-2013

Product Description	Garden Highway, fresh, Mango spears, packed in its Own Juice, Grown In: Mexico Net Wt 1 lb (454g), 1.5 lbs(680 g); 2 lbs (32 oz); Delish Mango Spears (5 oz, 1 lb) for Walgreens ; Generic Label Mango Spears for Kroger (1 lb)
Code Info	Garden Fresh Item 383022, 383850, 383837, 1 lb, 1.5 lb, 2 lb, UPC 8.26766-26849.8, 8.26766-21406.8, 8.26766-25580.1 DeLish Item 5 oz item 383139, 0.49022-53700.2; 1 lb item 383113, 0.49022-58823.3; generic 1 lb item 383001, 8.26766-88058.4, Best By 8/04/2012- 09/16/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	14,711
Recall Number	F-0131-2013

Product Description	Tropical Fruit Medley, Ingredients Pineapple, Mango & Papaya; Garden Highway ( brand) Net Wt 1 lb, UPC 8.26766-26848.1 Trader Joe's, Nt. Wt. 16 oz (1 lb) 454 g, UPC 00949361 deLISH (brand) Nt. Wt. 10 oz.(285g), UPC 49022 53699
Code Info	Garden Highway Item 383006 Trader Joes item 383088 deLish item 383137 Best By 8/04/2012- 09/16/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	3930
Recall Number	F-0132-2013

Product Description	Garden Highway, Chef Essentials, Mango Salsa, Net Wt 7 oz, UPC 8.26766-42208.1, Ingredients: Mango, Lime Juice, Red Onion, Mint, Jalapeno Pepper, Packed in It's Own Juice
Code Info	Item 382987, Best By 8/04/2012- 09/16/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	7 cases
Recall Number	F-0133-2013

Product Description	Garden Highway,Chef Essentials fresh, Tropical Salsa, Net Wt 8 oz, UPC 8.26766-42195.4. Ingredients: Mango, Papaya, Red Onion, Pineapple, Red Bell Pepper, Lime Juice Cilantro, Jalapeno in its Own Juice
Code Info	Item 382986, Best By 8/04/2012- 09/16/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity
Recall Number	F-0134-2013

Product Description	Garden Highway,Watermelon Mango Medley, Net Wt 7oz, UPC 8.26766-24062.3, Ingredients: Watermelon, Mango, Blueberries in its Own Juice
Code Info	Item 383106, Best By 7/26/2012- 09/09/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	2 cases
Recall Number	F-0135-2013

Product Description	Fruit Tray, Generic Label Sold at Wal-Mart Stores, 1 lb 14 oz, UPC 8.26766-25588.7. Ingredients Pineapple, Apples,{ Apples calcium ascorbate (a blend of calcium and vitamins to maintain color)}, Cantaloupe, Mango, Grapes
Code Info	Item 383009, Best By 8/04/2012- 09/16/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity
Recall Number	F-0136-2013

Product Description	Seasonal Blend Fresh Fruit, 16 oz (1 lb), UPC 8.26766-25534.4 and 32 oz (2 lb), UPC 8.26766.26805.4.Generic Label Sold at Wal-Mart Stores Ingredients Pineapple, Cantaloupe, Honeydew, Strawberries, Grapes, Mango
Code Info	Item 383334 and 383477, Best if Sold by 8/04/2012- 09/16/12
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	8582
Recall Number	F-0137-2013

Product Description	Signature Cafe Fruit Basket Medley 30 oz (1 lb 14 oz), UPC 8.26766-06918, Ingredients Grapes,Pineapple, Cantaloupe, Mango, Watermelon, apples
Code Info	Item 383062, Use By SEP 1612
Classification	Class I
Reason for Recall	In cooperation with the FDA warning to not consume mangoes from Agricola Daniella, Mexico. FreshLine of Indianapolis, Indiana, has initiated a voluntary recall of a limited quantity of expired products that contain fresh-cut mangoes due to the potential risk that the mangoes may contain Salmonella.
Product Quantity	674
Recall Number	F-0138-2013

Class I Food/Cosmetics Event

Event ID	63213
Status	Terminated
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	17-Sep-12
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Liberty Fruit Co Inc - Carols Cuts Div
City	Kansas City
State	KS
Country	US
Distribution Pattern	Distribution was made to KS.

Associated Products

Product Description	Carol's Cuts, mangos cubed, item # 71035, packaged in 5-lb, black plastic tray, heat sealed with a film lid, single-use package. The responsible firm name on the label is Carol's Cuts, Kansas City, KS
Code Info	Lot number 81260-1824, use by date 9/2/2012
Classification	Class I
Reason for Recall	Product is potentially contaminated with Salmonella gaminara.
Product Quantity	185/5-lb trays
Recall Number	F-0111-2013

Class I Food/Cosmetics Event

Event ID	63217
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	10-Sep-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	Floyd Peterson Company Inc.
City	Auburn
State	WA
Country	US
Distribution Pattern	Product distributed to distributors, retailers, and restaurants in Oregon and Washington.

Associated Products

Product Description	Ricotta Salata Frescolina Brand Soft Cheese. Product is packaged in a retail package, wedge shaped, size ranges from 6-7 oz. The product is labeled in parts: "*Frescolina Ricotta Salata MARTEIMPORTED BY FOREVER CHEESE,NY 11106PRODUCT OF ITALY*"
Code Info	manufacturer codes 7022, 7212, 7272 and 7432.
Classification	Class I
Reason for Recall	Ricotta Salata Frescolina Brand Cheese is recalled due to the potential contamination with Listeria monocytonenes.
Product Quantity	total 390 lbs
Recall Number	F-0122-2013

Class I Food/Cosmetics Event

Event ID	63269
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	13-Sep-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	Specialty Commodities, Inc.
City	Fargo
State	ND
Country	US
Distribution Pattern	CA, GA, IL, MO, NY, TX, WA

Associated Products

Product Description	Macadamia Nuts Style 2, RAW, SHELLED. DESCRIPTION OF CARTON FROM GUATEMALA: LOT 2 70 JUNE 25/12 423, 43 1 NORMAL/BIG .
Code Info	Lot #: 275 & 271 BEST BEFORE MAY/14, 1427
Classification	Class I
Reason for Recall	Specialty Commodities Inc., is recalling product due to potential contamination with Salmonella.
Product Quantity	27,350 lbs (1094- 25 lb cartons)
Recall Number	F-0124-2013

Class I Food/Cosmetics Event

Event ID	63274
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	18-Sep-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	World Food LLC.
City	Orlando
State	FL
Country	US
Distribution Pattern	Distributed throughout FL.

Associated Products

Product Description	Fresh Fruit Burst fruit cup, packaged in 1 and 1.5 lb containers. Labeled in part: "*Fruit BurstIngredients: Watermelon, Cantaloupe, Pineapple, Honeydew, Grapes, Mango, Blueberries. Packed in its own juice**"
Code Info	World Food Lot Code 011347 Best if Sold By: 09/13/12, 09/21/2012, 09/22/2012, 09/23/2012, 09/24/2012 UPC Code 21140-01701 and 21140-01707
Classification	Class I
Reason for Recall	On 09/18/2012, World Foods, LLC recalled various products containing mangoes supplied from Agricola Daniella with the potential to be contaminated with Salmonella.
Product Quantity	7220 lbs/1455 cases
Recall Number	F-0148-2013

Product Description	Mango Spears, packaged in 1 lb containers. Labeled in part: "*Mango SpearsIngredients: MangoPacked in its own juiceGrown in: Mexico **"
Code Info	World Food Lot Code 011347 Best if Sold By: 09/21/2012, 09/22/2012, UPC Code 21140-01694
Classification	Class I
Reason for Recall	On 09/18/2012, World Foods, LLC recalled various products containing mangoes supplied from Agricola Daniella with the potential to be contaminated with Salmonella.
Product Quantity	244 lbs/ 61 cases
Recall Number	F-0149-2013

Product Description	Fresh Island Medley, packaged in 1 lb containers. Labeled in part: "*Island MedleyIngredients: Pineapple, Mango, PapayaPacked in its own juice**"
Code Info	World Food Lot Code 011347 Best if Sold By: 09/13/2012, 09/21/2012, 09/22/2012, 09/23/2012 UPC Code 21140-01696
Classification	Class I
Reason for Recall	On 09/18/2012, World Foods, LLC recalled various products containing mangoes supplied from Agricola Daniella with the potential to be contaminated with Salmonella.
Product Quantity	700lbs/175 cases
Recall Number	F-0150-2013

Class I Food/Cosmetics Event

Event ID	63289
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	25-Sep-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	Publix Super Markets
City	Lakeland
State	FL
Country	US
Distribution Pattern	Florida, Georgia, South Carolina, Alabama, and Tennessee

Associated Products

Product Description	*PublixHearts of RomaineChopped Hearts of RomaineTriple Washed& Ready to EatNo PreservativesNET WT 10 OZ (284g)*
Code Info	Best if used by Sept 20
Classification	Class I
Reason for Recall	Listeria Monocytogenes in a sample collected by IEH and confirmed by FDA
Product Quantity	763 cases
Recall Number	F-0108-2013

Class I Food/Cosmetics Event

Event ID	63298
Status	Terminated
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	26-Sep-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	Gretchen's Shoebox Express
City	Seattle
State	WA
Country	US
Distribution Pattern	Product was distributed to retail stores in Washington.

Associated Products

Product Description	Evolution Fresh brand Cinnamon and Apple Almond Butter Sandwiches in plastic wrap, NET WT 5.75 oz., UPC 726111926371. Label reads in part, perishable. keep refrigerated. CINNAMON APPLE & ALMOND BUTTER SANDWICH; MANUFACTURED FOR EVOLUTION FRESH, INC.
Code Info	Enjoy by: 9/24/12, 9/25/12
Classification	Class I
Reason for Recall	The almond butter used to manufacture the product, supplied by Sunland, Inc., is potentially contaminated with Salmonella.
Product Quantity	12 units
Recall Number	F-0125-2013

Product Description	Evolution Fresh brand Almond Butter in individual 2-oz containers, UPC 726111926838. Label reads in part, perishable. keep refrigerated. ALMOND BUTTER, NET WT 2 OZ, MANUFACTURED FOR EVOLUTION FRESH, INC.
Code Info	Enjoy by: 9/25/12, 9/26/12, 10/2/12, 10/3/12, 10/7/12
Classification	Class I
Reason for Recall	The almond butter used to manufacture the product, supplied by Sunland, Inc., is potentially contaminated with Salmonella.
Product Quantity	8 units
Recall Number	F-0126-2013

Class I Food/Cosmetics Event

Event ID	63318
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	28-Sep-12
Initial Firm Notification of Consignee or Public	E-Mail

Recalling Firm	C.G. Higgins Confections, LLC
City	Santa Fe
State	NM
Country	US
Distribution Pattern	Retailers and end users located in NM, USA.

Associated Products

Product Description	Peanut Butter Fudge 3 oz bag, manufactured from 6-28-12 thru 9-20-12
Code Info	No manufacturing code.
Classification	Class I
Reason for Recall	Peanut Butter used to product Peanut Butter Fudge was recalled by Sunland, Inc.; therefore, this product has the potential to be contaminated with Salmonella.
Product Quantity	132 lbs
Recall Number	F-0140-2013

Class I Food/Cosmetics Event

Event ID	63320
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	27-Sep-12
Initial Firm Notification of Consignee or Public	E-Mail

Recalling Firm	Newman's Own Organics
City	Aptos
State	CA
Country	US
Distribution Pattern	The product is distributed in the US only. Firm's distributors are location nationwide: AZ, CA, CO, CT, GA, NH, IA, IL, IN, NJ, NV, OR, PA, TN, TX, WA. However, the firm's distributors service a large area and can ship to retailers outside of their state.

Associated Products

Product Description	Newman's Own Organics brand Newman-O's Peanut Butter Creme Filled Chocolate Cookies 8oz/6 pack, Unit UPC#7 57645 02170 8, Case UPC#7 57645 02171 5; 13oz/6 pack, Unit UPC# 7 57645 02150 0, Case UPC#7 57645 02151 7; 9oz/6 pack, Unit UPC#7 57645 02288 0, Case UPC # 7 57645 02388 7; 16oz/ 12 pack, Unit UPC# 7 57645 02239 2, Case UPC # 7 57645 02339 9; Product is manufactured by J&J Snack Foods, 5353 Downey Rd., Vernon, CA and distributed by Newman's Own Organics, Aptos, CA
Code Info	Expiration Dates: 11/26/10 and later
Classification	Class I
Reason for Recall	The product was manufactured using peanut butter recalled by Sunland Inc. and it may be contaminated with Salmonella.
Product Quantity	4,609 cases or 27,654 packages total
Recall Number	F-0292-2013

Class I Food/Cosmetics Event

Event ID	63339
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	02-Oct-12
Initial Firm Notification of Consignee or Public	E-Mail

Recalling Firm	Whole Foods Market Group Inc.
City	Everett
State	MA
Country	US
Distribution Pattern	Massachusetts, Rhode Island, Maine, Connecticut, New York and New Jersey

Associated Products

Product Description	Whole Foods Roasted Garlic Eggplant Soup , 24oz plastic container UPC: 3640630269
Code Info	Sell By: October 14 2012
Classification	Class I
Reason for Recall	Product labeled as Whole Foods Roasted Garlic and Eggplant Soup may contain Lobster Corn Bisque. Undeclared allergens: Shellfish, Milk
Product Quantity	360/24 oz
Recall Number	F-0290-2013

Class I Food/Cosmetics Event

Event ID	63340
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	02-Oct-12
Initial Firm Notification of Consignee or Public	Press Release

Recalling Firm	Gretchen's Shoebox Express
City	Seattle
State	WA
Country	US
Distribution Pattern	Product was distributed at cafe stores in Oregon and Washington only. There are no Canadian consignees.

Associated Products

Product Description	Starbuck Protein Bistro Box, 6.80 oz. package, UPC 762111881502. The Starbuck Protein Bistro Box contains the 0.5 oz. single-serve Honey Peanut Butter Blend squeeze pack with the UPC 894455000391.
Code Info	Enjoy By dates: 09/02/12 to 09/27/12, 9/28/12, 9/30/12-10/6/12. The 0.5 oz. single-serve Honey Peanut Butter squeeze pack has the Best By dates: 7/14/13, 8/10/13, 8/13/13, 8/14/13, 8/15/13, and/or 8/26/13.
Classification	Class I
Reason for Recall	The 0.5 oz. single-serve Honey Peanut Butter squeeze packs in the Starbuck Protein Bistro Boxes containing peanut that has a potential to be contaminated with Salmonella.
Product Quantity	approximately 16, 752 units
Recall Number	F-0139-2013

Class I Food/Cosmetics Event

Event ID	63342
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	28-Sep-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Late July Snacks, LLC
City	Barnstable
State	MA
Country	US
Distribution Pattern	Nationwide

Associated Products

Product Description	Late July Organic Mini Peanut Butter Sandwich Crackers packaged in : 5oz box UPC 890444000700 8ct carton/1.125oz (single serve caddy) & 1.125oz pack (single serve pack UPC: 890444000724 & 890444000717
Code Info	5 oz: 19MAY13 through 11JUL13 (stamped on box of bottom) 8ct carton/1.125oz (single serve caddy) & 1.125oz pack (single serve pack): 15JUN13 through 10JUL13 (code is stamped on each individual pack or on the end of the carton)
Classification	Class I
Reason for Recall	Organic Mini Peanut Butter Sandwich Crackers are recalled due to Sunland peanut butter recall due to the potential to be contaminated with Salmonella
Product Quantity	12,681 cases
Recall Number	F-0291-2013

Class I Food/Cosmetics Event

Event ID	63388
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	05-Oct-12
Initial Firm Notification of Consignee or Public	Press Release

Recalling Firm	Kilwin's Quality Confections, Inc.
City	Petoskey
State	MI
Country	US
Distribution Pattern	Michigan and Florida Distribution centers with Retail stores in Florida, Georgia, Indiana, Michigan, North Carolina, Ohio, South Carolina, Tennessee, and Wisconsin receiving product.

Associated Products

Product Description	Kilwins Sugar Free S/F PEANUT BUTTER FUDGE, Nt. Wt. 7-oz (198 g)
Code Info	Item 648, bar code 000648, lots 67936, 67105, 66959, 66413, 66248, 65123, 63124, 62693, 62612, 61658, 61621
Classification	Class I
Reason for Recall	The peanut butter ingredient used to make the product is associated with the Sunland, Inc. recall and has the potential to be contaminated with Salmonella.
Product Quantity	640 pkgs (160 four count cases)
Recall Number	F-0141-2013

Class II Biologics Event

Event ID	40327
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	28-Dec-04
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Ogden Medical Center, Inc.
City	Ogden
State	UT
Country	US
Distribution Pattern	UT, Switzerland

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	7060020
Classification	Class II
Reason for Recall	Blood products, which were collected from a donor who traveled to a malarial endemic area, were distributed.
Product Quantity	1 unit
Recall Number	B-2422-12

Class II Biologics Event

Event ID	40858
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	11-Oct-05
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Poudre Valley Health Care, Inc
City	Fort Collins
State	CO
Country	US
Distribution Pattern	CO, NJ

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	8623753; 8624162
Classification	Class II
Reason for Recall	Blood products, which were collected from a donor who traveled to malarial endemic areas, were distributed.
Product Quantity	2 units
Recall Number	B-2417-12

Class II Biologics Event

Event ID	40965
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	02-Nov-05
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Poudre Valley Health Care, Inc
City	Fort Collins
State	CO
Country	US
Distribution Pattern	CO, NJ

Associated Products

Product Description	Fresh Frozen Plasma
Code Info	8623581
Classification	Class II
Reason for Recall	Blood products, collected from a donor whose arm scrub may have been incorrectly performed, was distributed.
Product Quantity	1 unit
Recall Number	B-2428-12

Class II Biologics Event

Event ID	42336
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	19-May-06
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	MO, CA.

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W045006028414
Classification	Class II
Reason for Recall	Blood products, which were collected from a donor who traveled to a malarial endemic area, were distributed.
Product Quantity	1 Unit
Recall Number	B-2443-12

Class II Biologics Event

Event ID	47615
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	07-Feb-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	Missouri

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W045008901224 (Part A); W045008901224(Part B)
Classification	Class II
Reason for Recall	Blood products, with positive bacterial detection testing, were distributed.
Product Quantity	2 Units
Recall Number	B-2456-12

Class II Biologics Event

Event ID	47616
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	11-Feb-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	Kansas

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W045008901655(Part A); W045008901655(Part B)
Classification	Class II
Reason for Recall	Blood Products, which were contaminated with Aspergillus versicolor, were distributed.
Product Quantity	2 Units
Recall Number	B-2511-12

Class II Biologics Event

Event ID	47617
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	27-Feb-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	Kansas; Missouri

Associated Products

Product Description	Fresh Frozen Plasma
Code Info	W045008902885
Classification	Class II
Reason for Recall	Blood Products, which were contaminated with Aspergillus versicolor, were distributed.
Product Quantity	1 Unit
Recall Number	B-2512-12

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W045008902885
Classification	Class II
Reason for Recall	Blood Products, which were contaminated with Aspergillus versicolor, were distributed.
Product Quantity	1 Unit
Recall Number	B-2513-12

Class II Biologics Event

Event ID	47619
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	22-Feb-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	Missouri; Kansas

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W045008902809
Classification	Class II
Reason for Recall	Blood products, which were possibly contaminated with Propionibacterium species, were distributed.
Product Quantity	1 Unit
Recall Number	B-2508-12

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W045008902809
Classification	Class II
Reason for Recall	Blood products, which were possibly contaminated with Propionibacterium species, were distributed.
Product Quantity	1 Unit
Recall Number	B-2509-12

Class II Biologics Event

Event ID	47981
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	25-Mar-08
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Community Blood Bank of Lancaster County Medical Society
City	Lincoln
State	NE
Country	US
Distribution Pattern	NE; Austria

Associated Products

Product Description	Blood and Blood Products for Reprocessing
Code Info	9128014
Classification	Class II
Reason for Recall	Blood products, collected from a donor with a history of Hepatitis A, were distributed.
Product Quantity	1 unit
Recall Number	B-2415-12

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	9128014
Classification	Class II
Reason for Recall	Blood products, collected from a donor with a history of Hepatitis A, were distributed.
Product Quantity	1 unit
Recall Number	B-2416-12

Class II Biologics Event

Event ID	47984
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	18-Feb-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	Missouri

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced Irradiated
Code Info	W045008900034
Classification	Class II
Reason for Recall	Blood products, which did not meet the acceptable product specifications for release, was distributed.
Product Quantity	1 Unit
Recall Number	B-2427-12

Class II Biologics Event

Event ID	49294
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	03-Jul-08
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	Missouri

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W045007086237
Classification	Class II
Reason for Recall	Blood products, collected from a donor who was illiterate, were distributed.
Product Quantity	1 Unit
Recall Number	B-2446-12

Product Description	Fresh Frozen Plasma
Code Info	W045007086237
Classification	Class II
Reason for Recall	Blood products, collected from a donor who was illiterate, were distributed.
Product Quantity	1 Unit
Recall Number	B-2447-12

Class II Biologics Event

Event ID	49353
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	15-Jul-08
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	MO

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W045008039993
Classification	Class II
Reason for Recall	Blood product, collected from a donor whose health history screening was inadequately performed, was distributed.
Product Quantity	1 Unit
Recall Number	B-2448-12

Class II Biologics Event

Event ID	50605
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	23-Oct-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	American National Red Cross (The)
City	Dedham
State	MA
Country	US
Distribution Pattern	MA

Associated Products

Product Description	Red Blood Cells (Apheresis) Leukocytes Reduced
Code Info	004GE05195P1;004GE05195P2
Classification	Class II
Reason for Recall	Blood products, requiring testing for separator validation, were distributed without testing.
Product Quantity	2 units
Recall Number	B-2408-12

Class II Food/Cosmetics Event

Event ID	61291
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	17-Feb-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Sunshine Peanut Company
City	Jacksonville
State	FL
Country	US
Distribution Pattern	Product was distributed to distributors in CA, FL, NJ, and WA.

Associated Products

Product Description	Sunny Boy Peanut Butter. Product is labeled in part: 6/5 lb tubs- "SunnyBoy Creamy PEANUT BUTTER*Net Wt. 5lb. (2.27KG)INGREDIENTS: Peanuts, Dextrose, Contains less than 2% of the following: Salt, Partially Hydrogenated Oil (Rapeseed Cottonseed And/Or Mono-Diglycerides)Allergen Statement: CONTAINS PEANUTSSunshine Peanut Company Tampa, FL 33637 -- Driscoll product 1,344 cases Lot 111912 & 112012. 35 lb pail labeled in part: ""SunnyBoy Creamy PEANUT BUTTERNet Wt. 35lb. (15.89KG)INGREDIENTS: Peanuts, Dextrose, Contains less than 2% of the following: Salt, Partially Hydrogenated Oil (Rapeseed Cottonseed And/Or Mono-Diglycerides)Allergen Statement: CONTAINS PEANUTSSunshine Peanut Company Tampa, FL 33637* -- South Bay Correctional Facility, South Bay, FL (Good Source) 72 Pails Lot 112412.
Code Info	lot codes: 111912, 112012, 112412.
Classification	Class II
Reason for Recall	On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb.
Product Quantity	72 - 35lb pails; 1344 - 6/5lb Tubs.
Recall Number	F-0113-2013

Product Description	Sunny Boy Low Sodium/ Low Salt Peanut Butter. Product is labeled in part: 35 lb pail labeled in part: ""SunnyBoy LowSodium/LowSalt*PEANUT BUTTERNet Wt. 35lb. (15.89 KG)INGREDIENTS: Peanuts, Dextrose, Contains less than 2% of the following: Partially Hydrogenated Oil (Rapeseed Cottonseed And/Or Mono-Diglycerides)Allergen Statement: CONTAINS PEANUTSSunshine Peanut Company Tampa, FL 33637* US Food Service, Boca Raton, FL Lot 113012 Qty 846 pails.
Code Info	lot codes: 112312.
Classification	Class II
Reason for Recall	On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb.
Product Quantity	846 pails
Recall Number	F-0114-2013

Product Description	Sunny Boy NoSalt Peanut Butter. No label was provided by the firm for this product. Product would have been labeled in part: "*SunnyBoy CREAMY PEANUT BUTTERNet Wt. 35lb. (15.89KG)Product of USA*" Marion C.I. (US Food)Lot 112012 - 12 Pails shipped.
Code Info	lot code: 112012
Classification	Class II
Reason for Recall	On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb.
Product Quantity	12 pails
Recall Number	F-0115-2013

Product Description	Product is 1 oz Peanut Butter. 1 oz pouch labeled in part: "PEANUT BUTTER*Ingredients: Roaster Peanuts, Sugar, Stabilizer (Rapeseed Cottonseed and/or Soybean Oils), Salt.Allergen Warning: Contains PeanutsSunshine Peanut Company Jacksonville, FL 32204SP767" Case label - "200/1oz PEANUT BUTTERPRODUCT OF USA**" 200/1oz Pouch Lot 112312 - 150 cases shipped to FDC, Seatac, WA (Market Place). 500/1oz Pouch Lot 112312 - 57 cases shipped to Cheney Brothers. Ocala, FL.
Code Info	lot code: 112312
Classification	Class II
Reason for Recall	On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb.
Product Quantity
Recall Number	F-0116-2013

Product Description	Product is 2 oz Peanut Butter. 2 oz pouch labeled in part: "PEANUT BUTTER 2 oz. Pouch*Ingredients: Roaster Peanuts, Sugar, Hydrogenated Vegetable Oil, (Rapeseed Cottonseed and/or Soybean Oils), Salt.Allergen Warning: Contains PeanutsSunshine Peanut Company Jacksonville, FL 32204SP767" Case Label: "200/ 2oz PouchPEANUT BUTTERSUNSHINE PEANUT CO.JACKSONVILLE, FL. 32204*" -- 200/2oz Lot 112312, 112412, 120112 406 shipped to Harvest Farms, Lancaster, CA.
Code Info	lot code: 112312, 112412, 120112.
Classification	Class II
Reason for Recall	On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb.
Product Quantity	406 cases
Recall Number	F-0117-2013

Product Description	Product is 50 lb Bag Peanut Butter. Product Case is labeled in part: "*50 Lbs BagPEANUT BUTTERPRODUCT OF USA* 50 Lb Bag Lot 113112 - 225 boxes shipped to Cheney Brothers, Ocala, FL. ----------- 10/5 Lbs Bag Peanut Butter. Product Case is labeled in part: "*10/5 Lbs Bag PEANUT BUTTERPRODUCT OF USA**" 10 / 5 Lb Bags Lot 113112 - 48 boxes shipped to Cheney Brothers, Ocala, FL.
Code Info	lot code: 113112.
Classification	Class II
Reason for Recall	On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and Sunshine Peanut Brand Peanut Butter, Codes 112012, 112312, 112412, 113112, and 120112. Routine sampling by USDA found the products to contain Aflatoxin levels greater than 20 ppb.
Product Quantity	48 boxes (10/5 Lb Bags) & 225 boxes (50 Lb Bags)
Recall Number	F-0118-2013

Class II Food/Cosmetics Event

Event ID	62280
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	04-Jun-12
Initial Firm Notification of Consignee or Public	Visit

Recalling Firm	Sun Boricua Pa'l Mundo Inc.
City	Camuy
State	PR
Country	US
Distribution Pattern	Puerto Rico only

Associated Products

Product Description	"Tacos de Langosta" (Lobster-filled turnovers)*Keep Refrigerated*Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebrada, Camuy PR 00627
Code Info	6-3-13, 2-4-13, 3-4-13, 13-4-13, 2-5-13, 1-6-13
Classification	Class II
Reason for Recall	Undeclared color additives: FD&C Yellow #5, Yellow #6 and Red #40.
Product Quantity	36,000 units
Recall Number	F-0293-2013

Product Description	"Tacos de Jueyes" (Crabmeat-filled turnovers)*Keep Refrigerated*Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebrada, Camuy PR 00627
Code Info	6-3-13, 7-3-13, 16-3-13, 28-3-13, 2-4-13, 3-4-13, 1-5-13, 28-5-13
Classification	Class II
Reason for Recall	Undeclared color additives: FD&C Yellow #5, Yellow #6 and Red #40.
Product Quantity	48,000 units
Recall Number	F-0294-2013

Product Description	"Tacos de Marlin" (Marlin-filled turnovers)*Keep Refrigerated*Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebrada, Camuy PR 00627
Code Info	3-3-13, 5-3-13, 6-3-13, 1-5-13, 2-5-13, 1-6-13
Classification	Class II
Reason for Recall	Undeclared color additives: FD&C Yellow #5, Yellow #6 and Red #40.
Product Quantity	36,000 units
Recall Number	F-0295-2013

Product Description	"Tacos de Camarones" (Shrimp-filled turnovers)*Keep Refrigerated*Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebrada, Camuy PR 00627
Code Info	3-3-13, 7-3-13, 16-3-13, 29-3-13, 3-4-13, 4-4-13, 1-5-13, 2-5-13, 1-6-12
Classification	Class II
Reason for Recall	Undeclared color additives: FD&C Yellow #5, Yellow #6 and Red #40.
Product Quantity
Recall Number	F-0296-2013

Class II Devices Event

Event ID	62569
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	20-Apr-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Osteotech Inc
City	Eatontown
State	NJ
Country	US
Distribution Pattern	Worldwide Distribution - USA (nationwide) and Internationally.

Associated Products

Product Description	Grafton DBM Putty Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0083-2013

Product Description	Grafton DBM Gel Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0084-2013

Product Description	Grafton DBM Flex Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0085-2013

Product Description	Grafton DBM A-Flex Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0086-2013

Product Description	Grafton DBM Crunch Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0087-2013

Product Description	Grafton DBM Matrix PLF Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0088-2013

Product Description	Grafton DBM Matrix Strips Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0089-2013

Product Description	Grafton DBM Orthoblend Small Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0090-2013

Product Description	Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0091-2013

Product Description	Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0092-2013

Product Description	Optimum Expanse R Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0093-2013

Product Description	Optimum Expanse S Multiple sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and bone void filler in bony voids or gaps of the skeletal system (ie spine, pelvis and extremeties) not intrinsic to the stability of the bony structure. The voids or gaps may be surgically created defects or effects created by traumatic injury to the bone.
Code Info	510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
Classification	Class II
Reason for Recall	Multiple lots of GRAFTON ® and XPANSE ®, which are used for bone grafting procedures are being recalled because there is a possibility that sterility of the outer surface of the inner pouch may become compromised.
Product Quantity	79,207 units for all products in recall event
Recall Number	Z-0094-2013

Class II Biologics Event

Event ID	62584
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	06-Jul-12
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Blood Assurance Inc
City	Chattanooga
State	TN
Country	US
Distribution Pattern	Tennessee; North Carolina; Indiana

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W043212020538; W043211042995;
Classification	Class II
Reason for Recall	Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
Product Quantity	2
Recall Number	B-2304-12

Product Description	Blood and Blood Products for Reprocessing
Code Info	W043212020538; W043211042995;
Classification	Class II
Reason for Recall	Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
Product Quantity	2
Recall Number	B-2305-12

Class II Biologics Event

Event ID	62602
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	06-Jul-12
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Our Lady Of The Lake Hospital Inc
City	Baton Rouge
State	LA
Country	US
Distribution Pattern	Louisiana

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W165712013005R;
Classification	Class II
Reason for Recall	Blood product, collected from a donor who reported travel to an area possibly endemic for malaria, was distributed.
Product Quantity	1
Recall Number	B-2374-12

Class II Biologics Event

Event ID	62620
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	31-May-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	HCSC-Blood Center
City	Bethlehem
State	PA
Country	US
Distribution Pattern	Pennsylvania

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced Irradiated
Code Info	W050912011533;
Classification	Class II
Reason for Recall	Blood products, collected from a donor whose medical history screening was incomplete, were distributed.
Product Quantity	1
Recall Number	B-2376-12

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W050912011533;
Classification	Class II
Reason for Recall	Blood products, collected from a donor whose medical history screening was incomplete, were distributed.
Product Quantity	1
Recall Number	B-2377-12

Class II Biologics Event

Event ID	62630
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	21-Jun-12
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	LifeSouth Community Blood Centers, Inc.
City	Gainesville
State	FL
Country	US
Distribution Pattern	Alabama

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W115112181422P; W115112181422P (split product)
Classification	Class II
Reason for Recall	Blood products, labeled leukoreduced without assurance that they met the criteria for leukoreduced products, were distributed
Product Quantity	2
Recall Number	B-2378-12

Class II Biologics Event

Event ID	62632
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	13-Jun-12
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	LifeSouth Community Blood Centers Inc - Birmingham Region
City	Birmingham
State	AL
Country	US
Distribution Pattern	Alabama

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W1151121927911;
Classification	Class II
Reason for Recall	Blood product, with platelet count below the specified minimum requirement, was distributed.
Product Quantity	1
Recall Number	B-2380-12

Class II Biologics Event

Event ID	62633
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	11-Jun-12
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	LifeSouth Community Blood Centers Inc - Birmingham Region
City	Birmingham
State	AL
Country	US
Distribution Pattern	Alabama

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W115112192067K;
Classification	Class II
Reason for Recall	Blood product, with platelet count below the specified minimum requirement, was distributed.
Product Quantity	1
Recall Number	B-2381-12

Class II Biologics Event

Event ID	62634
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	13-Jun-12
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	LifeSouth Community Blood Centers Inc - Birmingham Region
City	Birmingham
State	AL
Country	US
Distribution Pattern	Alabama

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W115112192059K;
Classification	Class II
Reason for Recall	Blood product, with platelet count below the specified minimum requirement, was distributed.
Product Quantity	1
Recall Number	B-2382-12

Class II Biologics Event

Event ID	62739
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	26-Jun-12
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Tri-counties Blood Bank
City	San Luis Obispo
State	CA
Country	US
Distribution Pattern	California

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced Irradiated
Code Info	W1428124064601 Part 1; W1428124064601 Part 2;
Classification	Class II
Reason for Recall	Blood products, which were labeled as leukoreduced, but were not tested to verify the White Blood Cell count, were distributed.
Product Quantity	2
Recall Number	B-2477-12

Class II Biologics Event

Event ID	62742
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	11-Jul-12
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center of Carolinas
City	Charlotte
State	NC
Country	US
Distribution Pattern	North Carolina

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W227012003998 Part 1 ; W227012003998 PART 2;
Classification	Class II
Reason for Recall	Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity	2
Recall Number	B-2482-12

Class II Biologics Event

Event ID	62808
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	21-Jun-12
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	LifeSouth Community Blood Centers, Inc.
City	Dunwoody
State	GA
Country	US
Distribution Pattern	Georgia

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W115112199093F;
Classification	Class II
Reason for Recall	Blood products, which were labeled as leukoreduced, but were not tested to verify the White Blood Cell count, were distributed.
Product Quantity	1
Recall Number	B-2485-12

Class II Biologics Event

Event ID	62809
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	18-Apr-12
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Blood Systems, Inc.
City	Reno
State	NV
Country	US
Distribution Pattern	Nevada, Arizona, Mississippi

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	W041911037651K; WO419110435677; W041912003080G; W0419120020419; W041912002091Q; W041911040658C;
Classification	Class II
Reason for Recall	Blood products, with insufficient plasma volume to support the platelet yield, were distributed.
Product Quantity	6
Recall Number	B-2486-12

Class II Food/Cosmetics Event

Event ID	62831
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	07-Aug-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Ernesto Tropical Food, Inc
City	Ponce
State	PR
Country	US
Distribution Pattern	Puerto Rico only (distributors and retailers in the local area)

Associated Products

Product Description	"Sofrito a Mi Gusto*100% Natural (Natural Seasoning)Keep RefrigeratedElaborado y Envasado por Ernesto Tropical Foods, Inc. Guadalupe#62 Ponce, Puerto Rico 00731*"
Code Info	TBD
Classification	Class II
Reason for Recall	Undeclared allergens: FD&C Yellow #5
Product Quantity	576 units
Recall Number	F-0142-2013

Product Description	"Recaito Doña Tita*Home Made StyleKeep RefrigeratedElaborado y Envasado por Ernesto Tropical Foods, Inc. Guadalupe #62, Ponce PR 00731Net Weight: 14 oz**"
Code Info	5774, 5780, 5783, 5784, 5785, 5803, 5805, 5806, 5824, 5834, 5836, 5840, 5850, 5863, 5868, 5881, 5898, 5903, 5942, 5949, 3966, 5707, 5708, 5709
Classification	Class II
Reason for Recall	Undeclared allergens: FD&C Yellow #5
Product Quantity	528 units
Recall Number	F-0143-2013

Class II Devices Event

Event ID	63086
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	09-Jan-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	The Anspach Effort, Inc.
City	Palm Beach Gardens
State	FL
Country	US
Distribution Pattern	Worldwide Distribution - US (nationwide) and the countries of: Italy, Japan, Switzerland, Turkey and Taiwan.

Associated Products

Product Description	"*Electric Systems Foot ControlRx Only*" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
Code Info	Serial Numbers: E31305311301, E31305311302, E31305311303, E31305311304, E31305311401, E31305311402, E31305311403, E31305311404, E31305311405, E32305311201, E32305311202, E33305311501, E33305311502, E33305311504, and E33305311505
Classification	Class II
Reason for Recall	The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot control/foot pedal due to the Foot Control Cable lacking the shield connection from the cable to the connector body.
Product Quantity	16 units
Recall Number	Z-0074-2013

Product Description	"*Electric Systems Foot Control with Direction OnlyRx Only**" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
Code Info	Serial Numbers: E28305271001, E28305271002, E28305271003, E28305271004, E2830527100, E28305271006, E28305271007, E28305271008, E2830521009, E28305271010, E29305270901, E29305270902, E29305270903, E29305271101, E29305271102, E29305271103, E29305271104, E29305271105, E29305271106, E29305271107, E29,
Classification	Class II
Reason for Recall	The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot control/foot pedal due to the Foot Control Cable lacking the shield connection from the cable to the connector body.
Product Quantity	41 units
Recall Number	Z-0075-2013

Product Description	"*Electric Systems Foot Control with Direction and IrrigationRx Only**" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
Code Info	Serial Numbers: E3230327501, E32305327502, E32305327503, E32305327504, E32305327505, E32305327601, E32305327602, E32305327603, E32305327604, and E32305327605
Classification	Class II
Reason for Recall	The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot control/foot pedal due to the Foot Control Cable lacking the shield connection from the cable to the connector body.
Product Quantity	10 units
Recall Number	Z-0076-2013

Class II Devices Event

Event ID	63115
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	26-Jun-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Linvatec Corp. dba ConMed Linvatec
City	Largo
State	FL
Country	US
Distribution Pattern	Worldwide Distribution - USA including AZ, CA, CO, FL, GA, LA, MA, ME, MI, MN, NJ, NM, NY, PA, TX, UT, and WA. Internationally to BE, CA, ES, MY, NZ and PL

Associated Products

Product Description	"*PressFT2.6 w/ Two #1 (4 metric) Hi-FiSuturesNP2622009-02CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA** To reattach soft tissue to bone in orthopedic surgical procedures
Code Info	Item number NP262
Classification	Class II
Reason for Recall	Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT HI-FI Sutures (items NP211, NP212, NP261, NP262, NP211H, NP261H-all lot numbers) due to the potential for the distal tip of the driver to become separated from the driver shaft after successful insertion of the implant.
Product Quantity	879 units for all products in recall event
Recall Number	Z-0063-2013

Product Description	"*PressFT2.6 w/ One #2 (5 metric) Hi-FiSutureNP2612009-02CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA** To reattach soft tissue to bone in orthopedic surgical procedures
Code Info	Item number NP261
Classification	Class II
Reason for Recall	Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT HI-FI Sutures (items NP211, NP212, NP261, NP262, NP211H, NP261H-all lot numbers) due to the potential for the distal tip of the driver to become separated from the driver shaft after successful insertion of the implant.
Product Quantity	879 units for all products in recall event
Recall Number	Z-0064-2013

Product Description	"*Press FT2.6 w/ One #2 (5 metric) Hi-FiSuture, HIPN22009-02CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA** To reattach soft tissue to bone in orthopedic surgical procedures
Code Info	Item number NP261H
Classification	Class II
Reason for Recall	Linvatec Corporation DBA ConMed Linvatec in Largo, FL is recalling Press FT HI-FI Sutures (items NP 211, NP 212, NP 261, NP 262, NP211H, NP261H-all lot numbers) due to the potential for the distal tip of the driver to become separated from the driver shaft after successful insertion of the implant.
Product Quantity	879 units for all products in recall event
Recall Number	Z-0065-2013

Product Description	"*PressFT2.1 w/ Two #0 (3.5 metric) Hi-FiSuturesNP2122009-02CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA** To reattach soft tissue to bone in orthopedic surgical procedures
Code Info	Item number NP212
Classification	Class II
Reason for Recall	Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT HI-FI Sutures (items NP211, NP212, NP261, NP262, NP211H, NP261H-all lot numbers) due to the potential for the distal tip of the driver to become separated from the driver shaft after successful insertion of the implant.
Product Quantity	879 units for all products in recall event
Recall Number	Z-0066-2013

Product Description	"*PressFT2.1 w/ One #2 (5 metric) Hi-FiSutureNP2112009-02CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA** To reattach soft tissue to bone in orthopedic surgical procedures
Code Info	Item number NP211
Classification	Class II
Reason for Recall	Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT HI-FI Sutures (items NP211, NP212, NP261, NP262, NP211H, NP261H-all lot numbers) due to the potential for the distal tip of the driver to become separated from the driver shaft after successful insertion of the implant.
Product Quantity	879 units for all products in recall event
Recall Number	Z-0067-2013

Product Description	NP211H*2009-02CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA** To reattach soft tissue to bone in orthopedic surgical procedures
Code Info	Item number NP211H
Classification	Class II
Reason for Recall	Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT HI-FI Sutures (items NP211, NP212, NP261, NP262, NP211H, NP261H-all lot numbers) due to the potential for the distal tip of the driver to become separated from the driver shaft after successful insertion of the implant.
Product Quantity	879 units for all products in recall event
Recall Number	Z-0068-2013

Class II Devices Event

Event ID	63124
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	13-Sep-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	Zimmer, Inc.
City	Warsaw
State	IN
Country	US
Distribution Pattern	Worldwide Distribution-USA (nationwide) including the states of Indiana and Oklahoma and the countries of Australia, Thailand, Malaysia, Germany, India, Bulgaria, Egypt, UK, Russian FED, Slovak, and Brazil.

Associated Products

Product Description	CPT Modular Stem, Item No. 00-8011-001-00; Lot 61947708. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplasty.
Code Info	Lot 61947708
Classification	Class II
Reason for Recall	Zimmer Inc. is initiating a removal of the CPT Modular Stem (item 00-8011-001-00), CPT Stem Petite (item 00-8011-000-05; ) and CPT Femoral Stem 12/14 Neck Taper Extended Offset,(item 00-8114-001-10 ) because devices were packaged in incorrect cartons and distributed internationally and domestically. Zimmer received five complaints of this packaging issue.
Product Quantity	59 both units
Recall Number	Z-0060-2013

Product Description	CPT Hip System Femoral Stem Petite, Item No. 00-8011-000-05. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplasty.
Code Info	Lot 62017554
Classification	Class II
Reason for Recall	Zimmer Inc. is initiating a removal of the CPT Modular Stem (item 00-8011-001-00), CPT Stem Petite (item 00-8011-000-05; ) and CPT Femoral Stem 12/14 Neck Taper Extended Offset,(item 00-8114-001-10 ) because devices were packaged in incorrect cartons and distributed internationally and domestically. Zimmer received five complaints of this packaging issue.
Product Quantity	20
Recall Number	Z-0061-2013

Product Description	CPT Femoral Stem 12/14 Neck Taper Extended Offset,(item 00-8114-001-10. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplasty.
Code Info	Item 00-8114-001-10, lots 61947699 and 61952551
Classification	Class II
Reason for Recall	Zimmer Inc. is initiating a removal of the CPT Modular Stem (item 00-8011-001-00), CPT Stem Petite (item 00-8011-000-05; ) and CPT Femoral Stem 12/14 Neck Taper Extended Offset,(item 00-8114-001-10 ) because devices were packaged in incorrect cartons and distributed internationally and domestically. Zimmer received five complaints of this packaging issue.
Product Quantity	59 both lots
Recall Number	Z-0062-2013

Class II Devices Event

Event ID	63155
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	11-Apr-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Beckman Coulter Inc.
City	Brea
State	CA
Country	US
Distribution Pattern	Worldwide Distribution - USA (nationwide) and the following countries: Argentina Australia Austria Belarus Belgium China Croatia Czech Republic Denmark Finland France Germany Hungary India Ireland Israel Italy Japan Korea, Republic of Kuwait Macao Malaysia Netherlands New Zealand Norway Panama Russian Federation Slovakia Slovenia South Africa Spain Sweden Switzerland Turkey United Kingdom

Associated Products

Product Description	AutoMate 1250 and AutoMate 2550, Part Numbers ODL25125 and ODL25255. The AutoMate 1200/2500 System Series is a semi-open, pre- and post-analytical sample processing and sorting system. The base system automates the sample sorting, decapping, and archiving processes. Handling and sorting of samples includes automatic detection of the tube type and cap type (color). Optional features include an Aliquot Module for creation of labeled secondary tubes (including the detection of the presence of adequate volume for the requested aliquots) and a Recapper Module to re-seal previously decapped tubes prior to archiving.
Code Info	All Serial Numbers
Classification	Class II
Reason for Recall	The recall was initiated because Beckman Coulter has confirmed customer reports of secondary tubes being labeled with two different barcode labels on the AutoMate 2500 Family (previously referred to as OLA2500 Systems) units which can cause misidentification of a sample when software versions lower than version 4.1 is used.
Product Quantity	468 units total (51 units in US)
Recall Number	Z-0056-2013

Class II Food/Cosmetics Event

Event ID	63159
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	10-Sep-12
Initial Firm Notification of Consignee or Public	E-Mail

Recalling Firm	Spartan Central Kitchen
City	Grand Rapids
State	MI
Country	US
Distribution Pattern	MI and OH only.

Associated Products

Product Description	Pound Cake 12 ounces
Code Info	All products with the sell by dates on or before Sept 21st.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	261
Recall Number	F-0151-2013

Product Description	#805 Salad - No Meat Asian 3/4 pounds
Code Info	All products with the sell by dates on or before September 13.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	99
Recall Number	F-0152-2013

Product Description	#804 Salad - No Meat Chicken Caesar 3/4 pounds
Code Info	All products with the sell by dates on or before September 13.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	131
Recall Number	F-0153-2013

Product Description	#803 Salad - No Meat 7 Layer 7/8 pounds
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	121
Recall Number	F-0154-2013

Product Description	#802 Salad - No Meat Large Chef 3/4 pounds #801 Salad - No Meat Small Chef 1/4 pound
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1) 141; 2) 132
Recall Number	F-0155-2013

Product Description	#767 Salad - Asian Chicken 3/4 pounds
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	437
Recall Number	F-0156-2013

Product Description	#766 Salad - Chicken Caesar 3/4 pounds
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	513
Recall Number	F-0157-2013

Product Description	#765 Salad - Seven Layer 7/8 pounds
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	678
Recall Number	F-0158-2013

Product Description	#764 Salad - Large Chef 3/4 pounds #763 Salad - Small Chef 1/4 pound
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1) 739; 2) 670
Recall Number	F-0159-2013

Product Description	#762 Salad - Large Garden Fresh 3/4 pounds #761 Salad - Small Garden Fresh 3 oz.
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1) 832; 2) 668
Recall Number	F-0160-2013

Product Description	#748 Chicken Spread Sandwich on White each
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	612
Recall Number	F-0161-2013

Product Description	#746 Sandwich - Turkey Cheddar each
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	468
Recall Number	F-0162-2013

Product Description	#745 Sandwich - Ham & Cheese sandwich
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	443
Recall Number	F-0163-2013

Product Description	#744 Sandwich - Sandwich Spread sandwich
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	653
Recall Number	F-0164-2013

Product Description	#743 Sandwich - Chicken Spread on Wheat each
Code Info	All with production dates 8/10/12 to 9/10/12 and UPC 0-11213-89999
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 10th to September 10th 2012 due to the possible contamination. No illnesses have been reported.
Product Quantity	725
Recall Number	F-0165-2013

Product Description	#742 Sandwich - Tuna Spread sandwich
Code Info	All with production dates 8/10/12 to 9/10/12 and UPC 0-11213-89998
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 10th to September 10th 2012 due to the possible contamination. No illnesses have been reported.
Product Quantity	686
Recall Number	F-0166-2013

Product Description	#741 Sandwich - Egg Salad on Wheat sandwich
Code Info	All with production dates 8/10/12 to 9/10/12 and UPC 0-11213-90011
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 10th to September 10th 2012 due to the possible contamination. No illnesses have been reported.
Product Quantity	764
Recall Number	F-0167-2013

Product Description	#705 Panini - Rotisserie Chicken sandwich
Code Info	All with production dates 8/10/12 to 9/10/12 and UPC 705
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 10th to September 10th 2012 due to the possible contamination. No illnesses have been reported.
Product Quantity	235
Recall Number	F-0168-2013

Product Description	#704 Panini - Reuben sandwich
Code Info	All with production dates 8/10/12 to 9/10/12 and UPC 704
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 10th to September 10th 2012 due to the possible contamination. No illnesses have been reported.
Product Quantity	215
Recall Number	F-0169-2013

Product Description	#703 Panini - Little Italy sandwich
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	305
Recall Number	F-0170-2013

Product Description	#702 Panini - American Club sandwich
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	316
Recall Number	F-0171-2013

Product Description	#701 Panini - California Turkey sandwich
Code Info	All products with the sell by dates on or before September 13th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	314
Recall Number	F-0172-2013

Product Description	#460 10 oz Broccoli Augratin 10 ounces
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	37
Recall Number	F-0173-2013

Product Description	#459 12 oz Sour Cream & Chive Redskin Potatoes 12 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	488
Recall Number	F-0174-2013

Product Description	#455 12 oz Fried Rice with Pineapple 12 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	292
Recall Number	F-0175-2013

Product Description	#451 12 oz Cheezy Potatoes 12 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	702
Recall Number	F-0176-2013

Product Description	#450 10 oz Garden Veggies 10 ounces
Code Info	All products with the sell by dates on or before September 15th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	360
Recall Number	F-0177-2013

Product Description	#449 10 oz Roasted Corn with Fresh Basil Butter 10 ounces
Code Info	All products with the sell by dates on or before September 15th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	325
Recall Number	F-0178-2013

Product Description	#448 10 oz Three Green Veggies 10 ounces
Code Info	All products witht he sell by dates on or before September 15th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	381
Recall Number	F-0179-2013

Product Description	#447 2 ct Bacon Twice Bake 12 ounces
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	331
Recall Number	F-0180-2013

Product Description	#446 2 ct Triple Cheese Twice Bake 12 ounces
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	406
Recall Number	F-0181-2013

Product Description	#445 12 oz Asiago & Artichoke Mashed Potatoes 12 ounces
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	59
Recall Number	F-0182-2013

Product Description	#443 10 oz Roasted Potatoes with Dill 10 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	481
Recall Number	F-0183-2013

Product Description	#442 10 oz Spinach Artichoke Manicotti 10 ounces
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	343
Recall Number	F-0184-2013

Product Description	#441 12 oz Spaghetti in Cherry Tomato Sauce 12 ounces
Code Info	All products with the sell by dates on or before September 15th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	332
Recall Number	F-0185-2013

Product Description	#440 12 oz Asparagus Linguini with Lemon Cream 12 ounces
Code Info	All products with the sell by dates on or before September 15th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	440
Recall Number	F-0186-2013

Product Description	#439 10 oz Very Green Pasta 12 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	414
Recall Number	F-0187-2013

Product Description	#438 10 oz Three Cheese Cheddar & Mac 10 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity
Recall Number	F-0188-2013

Product Description	#436 10 oz Italian Sausage Penne 10 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	377
Recall Number	F-0189-2013

Product Description	#429 10 oz Beef Burrito 10 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	547
Recall Number	F-0190-2013

Product Description	#427 10 oz Shepherd's Pie 10 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	951
Recall Number	F-0191-2013

Product Description	#426 08 oz Grilled Salmon w/Couscous 8 ounces
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1407
Recall Number	F-0192-2013

Product Description	#425 08 oz Tilapia w/Lemon Orzo
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1466
Recall Number	F-0193-2013

Product Description	#423 12 oz Shredded Chicken Enchilada 12 ounces
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	949
Recall Number	F-0194-2013

Product Description	#421 12 oz Chicken Parmesan w/Linguini each
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	992
Recall Number	F-0195-2013

Product Description	#416 MME Tilapia No Meat each
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	51
Recall Number	F-0196-2013

Product Description	#415 MME Grilled Salmon No Meat each
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	63
Recall Number	F-0197-2013

Product Description	#412 MME Coconut Chicken No Meat 8 ounces
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	40
Recall Number	F-0198-2013

Product Description	#411 MME Chicken Parmesan No Meat each
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	48
Recall Number	F-0199-2013

Product Description	#391 1/2 Roasted Vegetable Quiche 0.5 each
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	74
Recall Number	F-0200-2013

Product Description	#390 1/2 Ham Quiche 0.5 each
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	306
Recall Number	F-0201-2013

Product Description	#386 1/2 Farmer's Quiche 1/2 each
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	695
Recall Number	F-0202-2013

Product Description	#385 1/2 Asparagus Quiche 0.5 each
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	664
Recall Number	F-0203-2013

Product Description	#384 1/2 Broccoli Quiche 0.5 each
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	315
Recall Number	F-0204-2013

Product Description	#383 2 lb Shredded Chicken Enchilada & Rice 4 each
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	367
Recall Number	F-0205-2013

Product Description	#380 2 lb Hearty Mac & Beef 2 pounds
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	294
Recall Number	F-0206-2013

Product Description	#373 Nippy Cheese - Pre-Pack 9 ounces
Code Info	All products with the sell by dates on or before October 2nd.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	798
Recall Number	F-0207-2013

Product Description	#372 Fruit Dip - Pre-Pack 8 ounces
Code Info	All products with the sell by dates on or before September 29th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	517
Recall Number	F-0208-2013

Product Description	#371 Taco Layer Dip - 30 oz., #370 Taco Layer Dip, 15 oz.
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1) 865; 2) 3332
Recall Number	F-0209-2013

Product Description	#363 Cheddar Free Ham & Onion Cheeseball 12 ounces
Code Info	All products with the sell by dates on or before September 22nd.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1032
Recall Number	F-0210-2013

Product Description	#362 Ham & Onion Cheeseball 12 ounces
Code Info	All products with the sell by dates on or before September 22nd.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	4329
Recall Number	F-0211-2013

Product Description	#361 VG's Fat Free Caesar Dressing 5 pounds
Code Info	All products with the sell by dates on or before October 11th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	123
Recall Number	F-0212-2013

Product Description	#360 VG's Caesar Salad Dressing 5 pounds
Code Info	All products with the sell by dates on or before October 3rd.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	375
Recall Number	F-0213-2013

Product Description	#358 Savory Seasoning 5 pounds
Code Info	All products with the sell by dates on or before January 8th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	51
Recall Number	F-0214-2013

Product Description	#357 Egg Spread 5 pounds
Code Info	All products with the sell by dates on or before September 15th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	65
Recall Number	F-0215-2013

Product Description	#356 Tuna Spread 5 pounds
Code Info	All products with the sell by dates on or before September 15th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	14
Recall Number	F-0216-2013

Product Description	#354 Bacon Potato - 8 count Pan 8 each
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	128
Recall Number	F-0217-2013

Product Description	#353 Triple Cheese Potato - 8 count Pan 8 each
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	161
Recall Number	F-0218-2013

Product Description	#347 Sandwich Spread 5 pounds
Code Info	All products with the sell by dates on or before October 2nd.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	377
Recall Number	F-0219-2013

Product Description	#350 Olive Oil
Code Info	All with production dates 8/10/12 to 9/10/12
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	25
Recall Number	F-0220-2013

Product Description	#346 Mexicana Dip 5 pounds
Code Info	All products with the sell by date on or before October 11th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	351
Recall Number	F-0221-2013

Product Description	#345 Chili Con Queso Dip 5 pounds
Code Info	All products with the sell by dates on or before October 2nd.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	656
Recall Number	F-0222-2013

Product Description	#343 Dill Dip 5 pounds
Code Info	All products with the sell by dates on or before October 10th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	363
Recall Number	F-0223-2013

Product Description	#342 Vegetable Dip 5 pounds
Code Info	All products with the sell by dates on or before October 10th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	128
Recall Number	F-0224-2013

Product Description	#341 Spinach Dip 5 pounds
Code Info	All products with the sell by dates on or before October 2nd.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1014
Recall Number	F-0225-2013

Product Description	#340 Mashed Potatoes 5 pounds
Code Info	All products with the sell by dates on or before September 21st.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	957
Recall Number	F-0226-2013

Product Description	#338 Tortellini Primavera 5 pounds
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	93
Recall Number	F-0227-2013

Product Description	#337 Smoked Mozzerella Salad 5 pounds
Code Info	All products with the sell by dates on or before September 16th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	143
Recall Number	F-0228-2013

Product Description	#336 Spaghetti Salad 5 pounds
Code Info	All products with the sell by dates on or before September 25th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	733
Recall Number	F-0229-2013

Product Description	#335 Sunshine Salad 5 pounds
Code Info	All products with the sell by date on or before October 2nd.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	274
Recall Number	F-0230-2013

Product Description	#334 Ambrosia Salad 5 pounds
Code Info	All products with the sell by date on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	170
Recall Number	F-0231-2013

Product Description	#333 Caribbean Fruit Salad 5 pounds
Code Info	All products with the sell by date on or before October 2nd.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	203
Recall Number	F-0232-2013

Product Description	#332 Tuna Noodle Salad 5 pounds
Code Info	All products with the sell by dates on or before September 17th.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	347
Recall Number	F-0233-2013

Product Description	#331 Italian Rotini Salad 5 pounds
Code Info	All with sell by dates on or before 25-Sept with UPC 331
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	143
Recall Number	F-0234-2013

Product Description	#330 Neptune Salad 5 pounds
Code Info	All with sell by dates on or before 17-Sept with UPC 330
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	378
Recall Number	F-0235-2013

Product Description	#329 Three Bean Salad 5 pounds
Code Info	All with sell by dates on or before 2-Oct with UPC 329
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	382
Recall Number	F-0236-2013

Product Description	#328 Kay Macaroni Salad 5 pounds
Code Info	All with sell by dates on or before 29-Sept with UPC 328
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	445
Recall Number	F-0237-2013

Product Description	#327 Kay Potato Salad 5 pounds
Code Info	All with sell by dates on or before 1-Oct with UPC 327
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	477
Recall Number	F-0238-2013

Product Description	#326 Pot Pie Mix 5 pounds
Code Info	All with sell by dates on or before 16-Sept with UPC 326
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	951
Recall Number	F-0239-2013

Product Description	#324 Baked Beans 5 pounds
Code Info	All with sell by dates on or before 2-Oct with UPC 324
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	322
Recall Number	F-0240-2013

Product Description	#322 Chicken Salad Base 5 pounds
Code Info	All with sell by dates on or before 2-Oct with UPC 322
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	428
Recall Number	F-0241-2013

Product Description	#321 Sonoma Chicken Salad 321 5 pounds
Code Info	All with sell by dates on or before 16-Sep with UPC 321
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	381
Recall Number	F-0242-2013

Product Description	#320 Mediterranean Orzo Salad 320 5 pounds
Code Info	All with sell by dates on or before 17-Sep with UPC 320
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	168
Recall Number	F-0243-2013

Product Description	#319 Cherry Chicken Penne Salad 319 5 pounds
Code Info	All with sell by dates on or before 18-Sep with UPC 319
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	155
Recall Number	F-0244-2013

Product Description	#318 Grilled Chicken Pasta Salad 318 5 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 318
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	316
Recall Number	F-0245-2013

Product Description	#317 Ham & Cheese Salad 317 5 pounds
Code Info	All with sell by dates on or before 17-Sep with UPC 317
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	482
Recall Number	F-0246-2013

Product Description	#315 Greek Feta Pasta Salad 315 5 pounds
Code Info	All with sell by dates on or before 17-Sep with UPC 315
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	377
Recall Number	F-0247-2013

Product Description	#312 Seafood Pasta Salad 312 5 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 312
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	79
Recall Number	F-0248-2013

Product Description	#314 Parmesan Roasted Turkey Salad 314 5 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 314
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	105
Recall Number	F-0249-2013

Product Description	#311 Fruit & Nut Wild Rice Salad 311 5 pounds
Code Info	All with sell by dates on or before 16-Sep with UPC 311
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	37
Recall Number	F-0250-2013

Product Description	#309 Macaroni Salad, Old Fashioned 309 5 pounds
Code Info	All with sell by dates on or before 17-Sep UPC 309
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	454
Recall Number	F-0251-2013

Product Description	#308 Sour Cream Mac & Cheddar 308 5 pounds
Code Info	All with sell by dates on or before 17-Sep with UPC 308
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	659
Recall Number	F-0252-2013

Product Description	#306 Asian Style Cole Slaw 306 5 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 306
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	204
Recall Number	F-0253-2013

Product Description	#305 Homemade Cole Slaw 7 pounds
Code Info	All with sell by dates on or before 17-Sep with UPC 305
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	732
Recall Number	F-0254-2013

Product Description	#304 Bacon Cheddar Potato Salad 304 5 pounds
Code Info	All with sell by dates on or before 17-Sep with UPC 304
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	816
Recall Number	F-0255-2013

Product Description	#303 Red White & Bleu Potato Salad 5 pounds
Code Info	All with sell by dates on or before 16-Sep with UPC 303
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	259
Recall Number	F-0256-2013

Product Description	#302 Old Fashioned Potato Salad 302 5 pounds
Code Info	All with sell by dates on or before 17-Sep with UPC 302
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1590
Recall Number	F-0257-2013

Product Description	#301 Creamy Redskin Potato Salad 5 pounds
Code Info	All with sell by dates on or before 16-Sep with UPC 301
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1666
Recall Number	F-0258-2013

Product Description	#234 Bulk Watermelon 234 2.5 pounds and #050 Watermelon Tray 16 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 234 and 0-11213-90395
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	48 (Bulk) and 792 (Tray)
Recall Number	F-0259-2013

Product Description	#233 Bulk Pineapple Chunks, 3 pounds; #076 Pineapple Chunks Fruit Cup, 9 oz.
Code Info	sell by date 9/15/12
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	55
Recall Number	F-0260-2013

Product Description	#232 Bulk Honeydew 232 3 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 232
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	71
Recall Number	F-0261-2013

Product Description	#231 Bulk Cantalope 231 3 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 231
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	85
Recall Number	F-0262-2013

Product Description	#075 Fruit Cup: Mixed Fruit 15.8 ounces #066 Fruit Cup: Mixed Fruit 9 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90466 and 0-11213-90457.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	2559
Recall Number	F-0263-2013

Product Description	#073 Fruit Cup: Cantalope Honeydew 15.8 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90462
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	560
Recall Number	F-0264-2013

Product Description	#070 Fruit Cup: Honeydew 15.8 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90460
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	383
Recall Number	F-0265-2013

Product Description	#068 Fruit Cup: Cantalope 15.8 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90459
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	807
Recall Number	F-0266-2013

Product Description	#067 Fruit Cup: Pineapple Chunks 9 ounces #054 Cored Pineapple 16 ounces #076 Fruit Cup: Pineapple Chunks 15.8 ounces
Code Info	All with sell by dates on or before 15-Sepwith UPC 0-11213-90455, 0-11213-90399, and 0-11213-90456.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	4702 total
Recall Number	F-0267-2013

Product Description	#064 Fruit Cup: Cantaloupe Honeydew Water Straw 9 ounces
Code Info	All products with the sell by dates on or before 15-Sept with UPC 0-11213-90465
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1269
Recall Number	F-0268-2013

Product Description	#063 Fruit Cup: Cantaloupe Honeydew Watermelon 9 ounces
Code Info	All products with the sell by dates on or before 15-Sept with UPC 0-11213-90464
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1089
Recall Number	F-0269-2013

Product Description	#061 Fruit Cup:Cantalope,Honeydew,Grape,Strawberry 9 ounces
Code Info	All products with the sell by dates on or before 15-Sept with UPC 0-11213-90463
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1305
Recall Number	F-0270-2013

Product Description	#060 Fruit Cup Watermelon 9 ounces #072 Fruit Cup: Watermelon 15.8 ounces
Code Info	All products with the sell by dates on or before 15-Sept with UPC 0-11213-90458 and 0-11213-90461.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	1746
Recall Number	F-0271-2013

Product Description	#055 10" Party Tray with No Dip 30 ounces
Code Info	All products with the sell by dates on or before 15-Sept. with UPC 0-11213-90409
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	651
Recall Number	F-0272-2013

Product Description	#048 Mixed Fruit Tray 20 ounces and #049 Mixed Fruit Tray 42 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90393 and 0-11213-90394
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	2059 (20 oz tray) and 1461 (42oz tray)
Recall Number	F-0273-2013

Product Description	#033 Sugar Snap Peas 7 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90419
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	261
Recall Number	F-0274-2013

Product Description	#029 Snow Peas 7 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90417
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	235
Recall Number	F-0275-2013

Product Description	#027 Diced White Onions 6 ounces and #026 Diced Red Onions 6 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90415 and 0-11213-90414
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	492 (white onions) and 502 (red onions)
Recall Number	F-0276-2013

Product Description	#025 Diced Colored Peppers 9 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90413
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	485
Recall Number	F-0277-2013

Product Description	#024 Diced Pepper & Onions 9 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90412
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	494
Recall Number	F-0278-2013

Product Description	#023 Soup Starter 8 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90411
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	164
Recall Number	F-0279-2013

Product Description	#022 Salad Topper 8 ounces
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90410
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	443
Recall Number	F-0280-2013

Product Description	#020 Vegetable Tray with Dip - 3 lb 0-11213-08488 3 pounds #016 Vegetable Tray with Dip 0-11213-90381 30 ounces #013 Vegetable Bowl w/Dip - Large 0-11213-08487 1.5 pounds #012 Vegetable Bowl w/Dip 0-11213-08489 0.59 pounds
Code Info	All with sell by dates on or before 16-Sep with UPC 0-11213-08488, 0-11213-90381, 0-11213-08487, and 0-11213-08489.
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	3447
Recall Number	F-0281-2013

Product Description	#017 Vegetable Tray with No Dip 2 pounds
Code Info	All with sell by dates on or before 16-Sep with UPC 0-11213-90408
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	371
Recall Number	F-0282-2013

Product Description	#011 Zucchini Stir,Fry 0.75 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90380
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All products with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	520
Recall Number	F-0283-2013

Product Description	#010 Broccoli Stir Fry 0.75 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90378
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	534
Recall Number	F-0284-2013

Product Description	#009 Colored Peppers 0.76 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90377
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All products with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	595
Recall Number	F-0285-2013

Product Description	#008 Red-Yellow-Green Peppers, Onions 0.75 pounds
Code Info	All with sell by dates on or before 15-Sep with UPC 0-11213-90379
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All products with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	676
Recall Number	F-0286-2013

Product Description	#002 Broccoli, Cauliflower 0.75 pounds
Code Info	All with sell by dates on or before 16-Sep with UPC 0-11213-08490
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity	898
Recall Number	F-0287-2013

Product Description	#747 Egg Salad Sandwich on White
Code Info	Sell by 9/13/12
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity
Recall Number	F-0288-2013

Product Description	#052 and #053, Party Tray with Fruit and Dip, 30 and 50 oz.
Code Info	Sell by 9/15/12
Classification	Class II
Reason for Recall	During an FDA inspection, microbiological swabs were collected and the results found that 21 sub samples in zones 1, 2 & 3 are positive for Listeria Monocytogenes (L.M.), Listeria innocua (L.I.) or Listeria seeligeri (L.S.). The firm is voluntarily recalling all products manufactured from August 20th to September 10th 2012 due to the possible contamination. All lots with sell by dates on or before 11-OCT. No illnesses have been reported.
Product Quantity
Recall Number	F-0289-2013

Class II Devices Event

Event ID	63191
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	06-Jul-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Beckman Coulter Inc.
City	Brea
State	CA
Country	US
Distribution Pattern	Worldwide Distribution and US (nationwide) and the countries of China, France, Italy and Taiwan.

Associated Products

Product Description	Unicel Closed Tube Aliquotter (UCTA) for UniCel DxC 660i, UniCel DxC 680i, UniCel DxC 860i, UniCel DxC 880i Synchron Access Clinical Systems. Part Number A45853. Product Usage: The UniCel DxC Synchron Clinical Systems are fully automated, computer-controlled clinical chemistry analyzers designed for the in-vitro determination of a variety of general chemistries, therapeutic drugs, and other chemistries. Analysis can be performed on serum, plasma, urine, or cerebrospinal fluid (CSF) and whole blood (sample type is chemistry dependent).
Code Info	Serial Numbers: 547-574 (UCTA)
Classification	Class II
Reason for Recall	The recall was initiated because Beckman Coulter has confirmed that the current sample syringe pump drive assemblies installed on DxC Integrated ystem with UniCel Closted Tube Aliquotter (UCTA) serial numbers between 547 and 574 may cause a hardware motion error (ID0x08000501).
Product Quantity	18 units
Recall Number	Z-0059-2013

Class II Food/Cosmetics Event

Event ID	63192
Status	Terminated
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	29-Jun-12
Initial Firm Notification of Consignee or Public	Email

Recalling Firm	Lovin Oven, LLC
City	Azusa
State	CA
Country	US
Distribution Pattern	Nationwide in the US

Associated Products

Product Description	Earth's Best Organic Wheat Teething Biscuits, 6 pack, UPC # 23923-90015, HCG#C90615
Code Info	Lot Codes: 29JUL12, 14AUG12
Classification	Class II
Reason for Recall	Earth's Best is recalling Earth's Best Organic Wheat Teething Biscuits because it may contain very small metal fragments.
Product Quantity	8,904 units
Recall Number	F-0109-2013

Class II Food/Cosmetics Event

Event ID	63203
Status	Completed
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	07-Jun-12
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	SUNFRESH NATURAL LLC.
City	Passaic
State	NJ
Country	US
Distribution Pattern	Nationwide

Associated Products

Product Description	SunFresh Natural Pitted Prunes Net wt. 6 oz. Distributed by: Sunfresh Natural LLC, Passaic, NJ 07055 Please visit us at: www.sunfreshnatural.com
Code Info	No codes
Classification	Class II
Reason for Recall	Prunes contained Rhodamine B45170 as unapproved color. The product also contains sorbic acid and the product labeling does not declare this on the ingredient statement.
Product Quantity	1200 bags
Recall Number	F-0297-2013

Class II Food/Cosmetics Event

Event ID	63206
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	06-Sep-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Lehi Valley Trading Co.
City	Mesa
State	AZ
Country	US
Distribution Pattern	US States: AZ, NJ, NM, NJ, TX, LA, CA, WI, WA, VT, GA, and FL. No international distribution.

Associated Products

Product Description	Licorice Sticks sold under the following brand names: 1) Orange Patch Country Store Licorice Sticks, New Wt, 12 oz. Packaged in plastic bag; 2) Desert Delite Licorice Sticks, New Wt, 12 oz. Packaged in plastic bag; 3) 17th Street Market Licorice Sticks, New Wt, 12 oz. Packaged in plastic bag; 4) Flagstaff Farmers Market Farm Fresh Licorice Sticks, New Wt, 16 oz. Packaged in plastic bag; 5) Farmers Market Licorice Sticks, New Wt, 8 oz., Packaged in plastic bag; 6) AJ's Fine Foods Licorice Sticks, New Wt, 16 oz. Packaged in plastic bag; 7) Schneph Farms Licorice Sticks, New Wt, 8 oz. Packaged in plastic bag; 8) Carlo's Produce Licorice Sticks, New Wt, 16 oz. Packaged in plastic bag; 9) Emery's Berry Patch Licorice Sticks, New Wt, 16 oz. Packaged in plastic bag; 10) Ben Becnel's Fruit Outlet Licorice Sticks, New Wt, 8 oz. Packaged in plastic bag; 11) The Country Store Licorice Sticks, New Wt, 12 oz. Packaged in plastic bag; 12) Woody's SmokehouseLicorice Sticks, New Wt, 8 oz and 12 oz. Packaged in plastic bag; 13) Hubbell Trading Post National Historic Site Licorice Sticks, 8 oz; 14) El Rancho Marketplace Licorice Sticks, New Wt, 16 oz. Packaged in plastic bag; 15) Jacob Lake Inn Licorice Sticks, New Wt, 8 oz. Packaged in plastic bag; 16) S&T Enterprises Licorice Sticks, New Wt, 1 lb, Packaged in plastic bag; 17) Arizona Snack Company Licorice Sticks, New Wt, 12 oz, Packaged in plastic bag; 18) Upchurch Candy Licorice Sticks, New Wt, 1 lb, Packaged in plastic bag; 19) Power Road Farmers Market Licorice Sticks, New Wt, 1 lb, Packaged in plastic bag; 20) Mountain Top Licorice Sticks, New Wt, 8 oz, Packaged in plastic bag; 21) Linn's Licorice Sticks, New Wt, 12 oz, Packaged in plastic bag; 22) Rosabella's Garden Bakery Licorice Sticks, New Wt, 4 oz, Packaged in plastic bag; 23) DiiIorio Farms & Roadside Market Licorice Sticks, New Wt, 8 oz, Packaged in plastic bag; 24) Foster's Product and Corn Maze Licorice Sticks, New Wt, 12 oz, Packaged in plastic bag; 25) Carleton Farm ProduceLicorice Sticks, New Wt, 8 oz and 12 oz, Packaged in plastic bag; 26) High Valley Orchard Licorice Sticks, New Wt, 16 oz, Packaged in plastic bag; 27) Murray Farms Licorice Sticks, New Wt, 1 lb, Packaged in plastic bag; 28) Venison World.Com Licorice Sticks, New Wt, 8 oz, Packaged in plastic bag; 29) Panorama Orchards, Inc. Licorice Sticks, New Wt, 8 oz, Packaged in plastic bag; 30) Jay Country Store Licorice Sticks, New Wt, 1 lb, Packaged in plastic bag; 31) Klicker's Licorice Sticks, New Wt, 16 oz, Packaged in plastic bag; 32) Rosie's Farm Market Licorice Sticks, New Wt, 8 oz, Packaged in plastic bag; 33) Stowe Mercantile Licorice Sticks, New Wt, 16 oz, Packaged in plastic bag; 34) Venice Gourmet Licorice Sticks, New Wt, 16 oz, Packaged in plastic bag; 35) Ragged Point Licorice Sticks, New Wt, 4 oz, Packaged in plastic bag; 36) Rawhide at Wild Horse Pass Licorice Sticks, New Wt, 8 oz, Packaged in plastic bag; 37) Petty's Meat Market Licorice Sticks, New Wt, 8 oz, Packaged in plastic bag; 38) Fly High with Pax Snax Licorice Sticks, New Wt, 12 oz, Packaged in plastic bag; 39) Bulk Foods Licorice Sticks, New Wt, 12 oz, Packaged in plastic bag; 40) Guantanamo Bay Gourmet Licorice Sticks, New Wt, 12 oz, Packaged in plastic bag; 41) Newport Harbor Gourmet Licorice Sticks, New Wt, 12 oz, Packaged in plastic bag; 42) Omni Resort Amelia Island Plantation Licorice Sticks, New Wt, 8 oz, Packaged in plastic bag; 43) The Big Easy Licorice Sticks, New Wt, 12 oz, Packaged in plastic bag; 44) Baker's Bay Associates Licorice Sticks, New Wt, 1 lb, Packaged in plastic bag; 45) Arizona Beagle Rescue Licorice Sticks, New Wt, 8 oz, Packaged in plastic bag; 46) Thomas Family Farm Licorice Sticks, New Wt, 4 oz, Packaged in plastic bag;
Code Info	1) Lot 0080245 and 0082378; 2) Lot 0080004; 3) Lot 0078721, 0085067, and 0081239; 4) 0079221, 0087572, 0084904, 0085398, 0086739, 0087046, 0084165, 0080870, 0080624, and 0082512; 5) Lot 0081294 and 0084453; 6) Lot 0086594, 0085743, 0083970, and 0078875; 7) Lot 0082198; 8) Lot 0085611; 9) Lot 0084498 and 0087230; 10) Lot 0079267l; 11) Lot 0086428, 0084609, 0083481; 0080971, and 0082505; 12) Lot 0087053, 0085253, 0082141,12 oz lots: 0082104, 0087463, 0085694, 0081038, 0084133; 13) Lot 0082299, 0082831, and 0086308; 14) Lot 0086200; 15) Lot 0083767; 16) Lot 0079247, 0079882, 0079656, 0080974, 0080424, 0080162, 0082436, 0081929, 0082184, 0081669, 0081406; 17) Lot 0081455, 0087359, and 0085778; 18) Lot 0084625; 19) Lot 0080277 and 0085536; 20) Lot 0081641; 21) Lot 0087089, 0085763, and 0083603; 22) Lot 0081624; 23) Lot 0084818; 24) Lot 0083720 and 0085577; 25) Lot 0084051, 0084446636, and 0082785; 26) Lot 0082692; 27) Lot 0083835; 28) Lot 0082977; 29) Lot 0087130; 30) Lot 0081515 and 0086922; 31) Lot 0085107; 32) Lot 0087178, 0084560, 0085493, and 0083401; 33) Lot 0085201 and 0086876; 34) Lot 0086301; 35) Lot 0084388 and 0080814; 36) Lot 0080394 and 0082341; 37) Lot 0086413; 38) Lot 0085563, 0082279, and 0081286; 39) Lot 0082916, 0080326, 0082012, 0079777, 0085413, 0087392, 0084263; 40) Lot 081277 and 0079762; 41) Lot 0081875; 42) Lot 0085390; 43) Lot 0082072; 44) Lot 0086147 and 0079417; 45) Lot 0082142; 46) Lot 0087501 Amounts distributed: 1) 24/12oz bags; 2) 36/12oz bags; 3) 120/16oz bags; 5) 72/8oz bags; 6) 48/16oz bags; 7) 24/8oz bags; 8) 12/16oz bags; 9) 24/16oz bags; 10) 24/8oz bags; 11) 60/12oz bags; 12) 72/18oz bags, 60/12oz bags; 13) 72/8oz bags; 14) 12/16oz bags; 15) 24/8oz bags; 16) 132/1lb bags; 17) 36/12oz bags; 18) 12/1lb bags; 19) 24/1lb bags; 20) 24/8oz bags; 21) 36/12oz bags; 22) 24/4oz bags; 23) 24/8oz bags; 24) 24/12oz bags; 25) 24/12oz and 72/8oz bags; 26) 12/16oz bags; 27) 24/1lb bags; 28) 24/8oz bags; 29) 24/8oz bags; 30) 24/1lb bags; 31) 12/16oz bags; 32) 96/8oz bags; 33) 24/16oz bags; 34) 12/16oz bags; 35) 48/4oz bags; 36) 48/8oz bags; 37) -; 38) 36/12oz bags; 39) 81/12oz bags; 40) 24/12oz bags; 41) 12/12oz bags; 42) 24/8oz bags; 43) 12/12oz bags; 44) 24/1lb bags; 45) -; 46: 24/4oz bags;
Classification	Class II
Reason for Recall	We were notified by American Licorice Co. through email that levels above those allowed by the FDA were found during testing. We have voluntarily recalled our entire product purchased from them for the required time range.
Product Quantity	Amounts distributed are listed in code information.
Recall Number	F-0120-2013

Class II Food/Cosmetics Event

Event ID	63218
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	18-Sep-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	Ralcorp Frozen Bakery Products
City	Downers Grove
State	IL
Country	US
Distribution Pattern	Kentucky, Michigan, Ohio

Associated Products

Product Description	GFS Individually Wrapped Blueberry Muffins, 1.8 Ounce, in 80 count case, Net Weight 9 lb./4.1 kg; Manufactured for Gordon Food Service, Grand Rapids, MI 40546; UPC 0 009390-157700 9 Please note: there is no labeling on the individual muffin wrappers other than the code date. The product is sold for institutional/food service use only.
Code Info	on case: Reorder No. 577006, Baked 07/30/12, use by 07/30/2013; on muffin wrapper: 07/30/12
Classification	Class II
Reason for Recall	Some of the cases labeled as blueberry muffins actually contain banana nut muffins, resulting in undeclared tree nuts
Product Quantity	1,542 cases
Recall Number	F-0119-2013

Class II Devices Event

Event ID	63223
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	09-May-12
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Aesculap, Inc.
City	Center Valley
State	PA
Country	US
Distribution Pattern	Within the US, product was distributed to PA and TN.

Associated Products

Product Description	Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
Code Info	NQ083R
Classification	Class II
Reason for Recall	The manufacturer informed the recalling firm of a potential laser marking error in size identification on two Columbus 4-IN-1 Femoral Cutting Guide Instruments. The guides are correctly dimensioned, but the laser markings have been incorrectly etched.
Product Quantity	2
Recall Number	Z-0082-2013

Class II Devices Event

Event ID	63225
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	02-Oct-09
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Terumo Cardiovascular Systems Corporation
City	Ann Arbor
State	MI
Country	US
Distribution Pattern	Worldwide distribution: USA (nationwide) including states of: CA, MI, NC, NJ, PA, and WI;and country of: EUROPE.

Associated Products

Product Description	Terumo Backplate Replacement CXFVR 1500 Holder The Flexible venous Reservoir is mounted on the Backplate/Holder and secures the flexible reservoir by strategically placed mounting arms. Additionally, there are three port supports the user incorporates to position the lines that enter and exit the venous bag. The Backplate/Holder is designed to allow the user to move the port support location to accommodate different tubing circuit designs to permit mounting flexibility.
Code Info	No lot/serial number; Catalog number: PN 816280
Classification	Class II
Reason for Recall	Backplate reservoir holders were manufactured with an incorrect configuration of connector supports. The devices were manufactured and configured with two 3/8 inch and one ½ inch connector supports instead of one 3/8 inch and two ½ inch connector supports (See location of supports as # 7 and # 8 on backplate attachment). The backplates were manufactured as described in manufacturing instructions and drawings; however, the drawings were incorrect. The incorrect configuration was identified by company. Replacement support connectors were provided to customers that had been shipped the devices and all other units in inventory were corrected. The affected units were manufactured and distributed between January 2008 and May 2009. A notification of this correction was not reported to FDA at that time.
Product Quantity	33 units
Recall Number	Z-0071-2013

Class II Food/Cosmetics Event

Event ID	63245
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	20-Sep-12
Initial Firm Notification of Consignee or Public	Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recalling Firm	Oregon Ice Cream, LLC
City	Eugene
State	OR
Country	US
Distribution Pattern	Product was distributed to distribution centers in CA, CO, CT, IA, IN, NH, and PA.

Associated Products

Product Description	Alden's Cookies and Cream is an ice cream product. It is packaged in a 1.5 quart (48 oz) cup. The LID of the recalled product is labeled in parts:"*ORGANICAlden's ICE CREAMCOOKIES 'n CREAM1.5 QTS (1.42L)". The CUP of the recalled product is labeled in parts: "ORGANICAlden's ICE CREAMCHOLOCATE CHOCOLATE CHIPMFD. BY OREGON ICE CREAMEUGENE, OR 974021-800-282-2202www.aldensicecream.com". The INGREDIENTS' STATEMENT on the cup is labeled in parts: "ORGANIC MILK AND CREAM, ORGANIC EVAPORATED CANE JUICE, ORGANIC CHOCOLATE LIQUOR AND COCOA BUTTER, ORGANIC ALKALIZED COCOA, ORGANIC TAPIOCA SYRUP, ORGANIC PALM KERNEL OIL, ORGANIC VANILLA EXTRACTS, ORGANIC TAPIOCA STARCH, NON-GMO SOY LECITHIN, GUAR GUM, LOCUST BEAN GUM, XANTHAN GUM**".
Code Info	12243 printed at the bottom of the cup
Classification	Class II
Reason for Recall	Alden's Cookies and Cream was packaged in the wrong cup and a correct lid was used, but wheat was not declared on the finished product's label.
Product Quantity	1400 cases/3 cups
Recall Number	F-0298-2013

Class II Food/Cosmetics Event

Event ID	63250
Status	Terminated
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	05-Feb-12
Initial Firm Notification of Consignee or Public	Visit

Recalling Firm	Bottling LLC dba Pepsi Beverages Company
City	Phoenix
State	AZ
Country	US
Distribution Pattern	Arizona

Associated Products

Product Description	Diet Crush Orange Soda, 12 oz cans
Code Info	APR1612ttttPW011012 (tttt represents military time)
Classification	Class II
Reason for Recall	Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license issued by one of their licensed bottlers, Pepsi Beverages Company in Phoenix, Arizona. The bottler used new graphics on cans of product made with the previous formulation which is in the process of being discontinued.
Product Quantity	1791 cases
Recall Number	F-0121-2013

Class II Devices Event

Event ID	63255
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	19-Sep-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Trumpf Medical Systems, Inc.
City	Charleston
State	SC
Country	US
Distribution Pattern	Nationwide Distribution-USA (nationwide) including the states of AR, CA, CO, CT, FL, GA, IL, KS, MA, MI, MO, NC, NJ, NY, OH, SC, TX, UT, VT and WI.

Associated Products

Product Description	Helion and Xenion surgical lights, 501/01 series KLM lights. The surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.
Code Info	Ondal AC2000 serial range of the spring arms requiring rework: 0111 010 xxxxxx to 0111 066 xxxxx (010 to 066 = month 01/year 20000 to month 06/year 2006 xxxxxx = 5 digit serial number).
Classification	Class II
Reason for Recall	Incidents regarding fractures of the front joint of the spring arm have been reported.
Product Quantity	275 units
Recall Number	Z-0077-2013

Class II Food/Cosmetics Event

Event ID	63315
Status	Ongoing
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	24-Sep-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Richmond Baking of Georgia Inc
City	Alma
State	GA
Country	US
Distribution Pattern	AZ, CA, FL, HI, ID, IL, IN, KS, MI, NJ, OR, PA, TN, TX, VA and WA.

Associated Products

Product Description	MJM Tropical Treats, Tropical Shaped Grahams, Orange, Net Wt. 1 oz., MJM Marketing, Super Wholesome Grahams, P.O. Box 1477, Kailua Kona, HI 96745-1477.
Code Info	Lot code; 030813, Pouches coded: 13067GA12, 13067GA22, 13067GA32, 13067GA42, 13052 and 13067GA62.
Classification	Class II
Reason for Recall	Product contains undeclared allergen: Soy Lecithin.
Product Quantity	896 cases (150/1oz. packages per case)
Recall Number	F-0112-2013

Class II Devices Event

Event ID	63359
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	26-Sep-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	MOOG Medical Devices Group
City	Salt Lake City
State	UT
Country	US
Distribution Pattern	Nationwide Distribution including California

Associated Products

Product Description	*This recall is being conducted due to an incomplete recall for RES 57829* Curlin Infusion Administration Set, REF 340-4165, Sterile EO, The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric delivery of fluids used in Parenteral, Enteral, Epidural, Subcutaneous and Intravenous applications.
Code Info	Product Code/Lot Number: 340-4166/CF1022906; 340-4128-V/CRF10082001; 340-4165/CF1022905.
Classification	Class II
Reason for Recall	This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which was related to customers reporting unclearable Air-In-Line alarm with specific lot numbers of Curlin Administration Sets used with Curlin Ambulatory Infusion Pumps. The lots associated with this recall were inadvertently omitted from the original recall which has since been terminated by the FDA.
Product Quantity	12,000 sets
Recall Number	Z-0072-2013

Class II Devices Event

Event ID	63365
Status	Ongoing
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	25-Sep-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Teleflex Medical
City	Research Triangle Park
State	NC
Country	US
Distribution Pattern	Nationwide Distribution including the state of Nevada.

Associated Products

Product Description	Hem-o-lok Large Polymer Ligating Clips, REF #544240, Rx only, Sterile, Teleflex Medical, Research Triangle Park, NC 27709. Teleflex Medicals Hem-o-lok polymer ligating clips are single use, sterile, non-absorbable medial devices that have been designed to ligate vessels and tissue structures during various types of surgical procedures. Vessels and tissue structures in the range of 0.5 to 16 mm can be effectively ligated with Hem-o-lok clips.
Code Info	Catalog No. 544240, Lot #01E1200585
Classification	Class II
Reason for Recall	Product is being recalled due to the possibility that the tray may contain pinholes, compromising product sterility.
Product Quantity	126 units
Recall Number	Z-0078-2013

Class II Drugs Event

Event ID	63406
Status	Ongoing
Product Type	Drugs
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	05-Oct-12
Initial Firm Notification of Consignee or Public	E-Mail

Recalling Firm	Earthborn Products, Inc.
City	San Diego
State	CA
Country	US
Distribution Pattern	Nationwide

Associated Products

Product Description	Colloidal Silver, 100 ppm TDS, Natural Mineral Supplement, sold in a) 2 fl.oz (59.15 mL), b) 8 fl.oz (236.6 mL), c) 16 fl.oz (473.2 mL), d) 32 fl.oz (946.4 mL), e) 64 fl.oz (1.89 L), and f) 1 Gal. (3.78 L), Distributed by: Earthborn Products, San Diego, CA 92103.
Code Info	Lot #: 009-22-A011, 011-28-A011, 004-01-A012, 005-24-A012, 007-24-A012, and 008-08-A012.
Classification	Class II
Reason for Recall	Marketed Without An Approved NDA/ANDA: This product is being recalled because FDA issued a final rule establishing that all over-the-counter (OTC) drug products containing colloidal silver ingredients or silver salts for internal or external use are not generally recognized as safe and effective and are misbranded.
Product Quantity	161 gallons
Recall Number	D-009-2013

Class III Biologics Event

Event ID	40195
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	04-May-05
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Community Blood Bank of Lancaster County Medical Society
City	Lincoln
State	NE
Country	US
Distribution Pattern	NE

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	3697502
Classification	Class III
Reason for Recall	Blood product, viral testing performed, interpreted, or documented incorrectly, were distributed.
Product Quantity	1 unit
Recall Number	B-2410-12

Product Description	Platelets Pheresis Leukocytes Reduced Irradiated
Code Info	3697525; 3697482; 3697482
Classification	Class III
Reason for Recall	Blood product, viral testing performed, interpreted, or documented incorrectly, were distributed.
Product Quantity	3 units
Recall Number	B-2411-12

Product Description	Platelets Pheresis Leukocytes Reduced
Code Info	3697528(Part A); 3697528(Part B)
Classification	Class III
Reason for Recall	Blood product, viral testing performed, interpreted, or documented incorrectly, were distributed.
Product Quantity	2 units
Recall Number	B-2412-12

Class III Biologics Event

Event ID	41806
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	27-Mar-06
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	University of Colorado Hospital
City	Aurora
State	CO
Country	US
Distribution Pattern	CO

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced, irradiated
Code Info	09FF59915;09GJ67158
Classification	Class III
Reason for Recall	Blood products, which were labeled with incorrect or missing information were distributed.
Product Quantity	2 units
Recall Number	B-2431-12

Class III Biologics Event

Event ID	44021
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	11-Jan-07
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Mississippi Valley Regional Blood Center
City	Davenport
State	IA
Country	US
Distribution Pattern	Pennsylvania

Associated Products

Product Description	Platelets
Code Info	LM44607
Classification	Class III
Reason for Recall	Blood product, which was manufactured from whole blood units in which collection extended beyond the allowable time limits, was distributed.
Product Quantity	1 Unit
Recall Number	B-2430-12

Class III Biologics Event

Event ID	47618
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	19-Feb-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	Kansas

Associated Products

Product Description	Fresh Frozen Plasma
Code Info	W045007056807;W045007056809
Classification	Class III
Reason for Recall	Blood products, for which storage condition was outside the acceptable range, were distributed.
Product Quantity	2 Units
Recall Number	B-2507-12

Class III Biologics Event

Event ID	48854
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	13-May-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Bank of Lancaster County Medical Society
City	Lincoln
State	NE
Country	US
Distribution Pattern	NE

Associated Products

Product Description	Platelets Pheresis Leukocytes Reduced Irradiated
Code Info	W087908300822
Classification	Class III
Reason for Recall	Blood product, labels applied to blood unit or product with incorrect or missing information, was distributed.
Product Quantity	1 unit
Recall Number	B-2409-12

Class III Biologics Event

Event ID	49809
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	25-Aug-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	MO

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W045008045744
Classification	Class III
Reason for Recall	Blood product, manufactured without additive solution, was distributed.
Product Quantity	1 Unit
Recall Number	B-2449-12

Class III Biologics Event

Event ID	50642
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	07-Oct-08
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center Of Gtr KC
City	Kansas City
State	MO
Country	US
Distribution Pattern	Missouri

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W045008091475
Classification	Class III
Reason for Recall	Blood product, manufactured without additive solution, was distributed.
Product Quantity	1 Unit
Recall Number	B-2450-12

Class III Devices Event

Event ID	62516
Status	Completed
Product Type	Devices
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	15-Nov-11
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Sunquest Information Systems, Inc.
City	Tucson
State	AZ
Country	US
Distribution Pattern	Nationwide distribution

Associated Products

Product Description	Sunquest Laboratory : intended for use by professionals working in a clinical laboratory.
Code Info	Versions 6.4.0 and later
Classification	Class III
Reason for Recall	Online calculations may not be performed as expected or may yield results that are different than expected when the calculation module is called from the Online Entry (OEM) application for a subtest whose subcolumn number on the instrument online string is divisible by 10.
Product Quantity	127 sites
Recall Number	Z-0073-2013

Class III Biologics Event

Event ID	62635
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	21-Jun-12
Initial Firm Notification of Consignee or Public	Telephone

Recalling Firm	Community Blood Center
City	Dayton
State	OH
Country	US
Distribution Pattern	Ohio

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced Irradiated
Code Info	W035412042113;
Classification	Class III
Reason for Recall	Blood product, labeled with an extended expiration date following irradiation, was distributed.
Product Quantity	1
Recall Number	B-2383-12

Class III Drugs Event

Event ID	63224
Status	Ongoing
Product Type	Drugs
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	20-Sep-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Sandoz Incorporated
City	Broomfield
State	CO
Country	US
Distribution Pattern	Nationwide

Associated Products

Product Description	Children's Cetirizine HCl Chewable Tablets 5 mg, 30 count blister pack, Manufactured in India by Sandoz Private Ltd., for Sandoz Inc., Princeton, NJ NDC 0781-5283-64 --- ALSO sold under Major brand All Day Allergy Children's Cetirizine HCl 5 mg, 5 count blister pack, Major Pharmaceuticals, Livonia, MI NDC 0904-5878-33
Code Info	NDC 0781-5283-64 lots: BT2862, BT7986, BT7994, BW0652, CC1961, and CA3437; NDC 0904-5878-33 lot BW0665.
Classification	Class III
Reason for Recall	Impurity/Degradation; exceeded impurity specification at the 8 and 15 month time points (betacyclodextrin ester 1&2)
Product Quantity	67,937 x 30 tablet cartons; 24,640 x 5 tablet cartons
Recall Number	D-008-2013

Class III Food/Cosmetics Event

Event ID	63227
Status	Terminated
Product Type	Food/Cosmetics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	29-Mar-12
Initial Firm Notification of Consignee or Public	Letter

Recalling Firm	Southwind Foods LLC dba Great American Seafood Imports Co.
City	Vernon
State	CA
Country	US
Distribution Pattern	CA, AZ, TX

Associated Products

Product Description	Frozen Red Cod Fillet (Red Snapper) Individually Quick Frozen was labeled and identified as Snapper FILL IQF (ROCKFISH). 1/10 lb, code #14343.
Code Info	Lot#90595
Classification	Class III
Reason for Recall	Southwind Foods is recalling Frozen Snapper Fill IQF (Rock Fish) because it mislabeled and misleading.
Product Quantity	145 cases
Recall Number	F-0123-2013

Mixed Classification Biologics Event

Event ID	62740
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	24-Jul-12
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Blood Assurance Inc
City	Chattanooga
State	TN
Country	US
Distribution Pattern	Florida; Indiana

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W043211068074;
Classification	Class II
Reason for Recall	Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity	1
Recall Number	B-2478-12

Product Description	Recovered Plasma
Code Info	W043211068074;
Classification	Class III
Reason for Recall	Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity	1
Recall Number	B-2479-12

Mixed Classification Biologics Event

Event ID	62741
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	13-Jul-11
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Blood Assurance Inc
City	Chattanooga
State	TN
Country	US
Distribution Pattern	Tennessee; Indiana

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W043210092064;
Classification	Class II
Reason for Recall	Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity	1
Recall Number	B-2480-12

Product Description	Recovered Plasma
Code Info	W043210092064;
Classification	Class III
Reason for Recall	Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity	1
Recall Number	B-2481-12

Mixed Classification Biologics Event

Event ID	62743
Status	Terminated
Product Type	Biologics
Voluntary/Mandated	Voluntary: Firm Initiated
Recall Initiation Date	20-Jun-12
Initial Firm Notification of Consignee or Public	FAX

Recalling Firm	Blood Assurance Inc
City	Chattanooga
State	TN
Country	US
Distribution Pattern	South Carolina; New York; Indiana

Associated Products

Product Description	Red Blood Cells Leukocytes Reduced
Code Info	W043211038237; W043210095642;
Classification	Class II
Reason for Recall	Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed
Product Quantity	2
Recall Number	B-2483-12

Product Description	Recovered Plasma
Code Info	W043211038237; W043210095642;
Classification	Class III
Reason for Recall
Product Quantity	2
Recall Number	B-2484-12

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