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U.S. Department of Health and Human Services

Enforcement Report - Week of October 24, 2012

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Class I Devices Event

Event ID62879
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date03-Aug-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmEthicon Endo-Surgery Inc
CityCincinnati
StateOH
CountryUS
Distribution PatternWorldwide 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 DescriptionHemorrhoidal 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 InfoPPH01: 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
ClassificationClass I
Reason for RecallEthicon 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 Quantity157,881 devices
Recall NumberZ-0057-2013

Class I Food Event

Event ID63032
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date25-Aug-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmSplendid Products
CityBurlingame
StateCA
CountryUS
Distribution PatternNationwide distribution.
 

Associated Products

Product DescriptionDaniella Mangoes May be identified by Daniella sticker with a PLU code of 3114, 4051, 4311, 4584 or 4959.
Code InfoAll fruit had identifying stickers with label "Daniella" and one of the following PLU numbers: 3114, 4051, 4311, 4584 or 4959.
ClassificationClass I
Reason for RecallFirm 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 NumberF-2395-2012

Class I Food Event

Event ID63101
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date30-Aug-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmHarry and David Operations, Inc.
CityMedford
StateOR
CountryUS
Distribution PatternInternet sales to 44 states and the District of Columbia
 

Associated Products

Product DescriptionCushman's Fruit and Flower Basket
Code Info205 through 242 printed on the shipping container. The format of the lot code is ###2M, with ### representing the numbers 205 through 242.
ClassificationClass I
Reason for RecallDaniella brand mangoes recalled due to potential contamination with Salmonella. Firm used mangoes in their fruit baskets.
Product Quantity739 total for recall
Recall NumberF-0144-2013
Product DescriptionCushman's New All Fruit Basket
Code Info205 through 242 printed on the shipping container. The format of the lot code is ###2M, with ### representing the numbers 205 through 242.
ClassificationClass I
Reason for RecallDaniella brand mangoes recalled due to potential contamination with Salmonella. Firm used mangoes in their fruit baskets.
Product Quantity
Recall NumberF-0145-2013
Product DescriptionHarry and David Fresh Fruit Gift Basket and Fresh Fruit Gift Basket Deluxe
Code Info205 through 242 printed on the shipping container. The format of the lot code is ###2M, with ### representing the numbers 205 through 242.
ClassificationClass I
Reason for RecallDaniella brand mangoes recalled due to potential contamination with Salmonella. Firm used mangoes in their fruit baskets.
Product Quantity
Recall NumberF-0146-2013
Product DescriptionHarry and David and Cushman's Original Gift Baskets
Code Info205 through 242 printed on the shipping container. The format of the lot code is ###2M, with ### representing the numbers 205 through 242.
ClassificationClass I
Reason for RecallDaniella brand mangoes recalled due to potential contamination with Salmonella. Firm used mangoes in their fruit baskets.
Product Quantity
Recall NumberF-0147-2013

Class I Food Event

Event ID63149
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date16-Aug-12
Initial Firm Notification of Consignee or Public E-Mail
Recalling FirmJ & J Snack Foods Corporation
CityPennsauken
StateNJ
CountryUS
Distribution PatternNationwide
 

Associated Products

Product DescriptionLuigi'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 InfoBest 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
ClassificationClass I
Reason for RecallLuigi's Real Italian Ice Birthday Cake Flavor is mislabeled as "Dairy-Free".
Product Quantity25,948 CASES
Recall NumberF-0079-2013

Class I Food Event

Event ID63184
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date11-Sep-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmWhole Foods Market
CityAustin
StateTX
CountryUS
Distribution PatternNationwide to 21 states
 

Associated Products

Product DescriptionFrescolina 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 InfoFrescolina Ricotta Salata PLU 293427. Mitica Ricotta Salata PLU 294413. All with Sell by dates Oct 2, 2012.
ClassificationClass I
Reason for RecallWhole 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 QuantityApproximately 2500 lbs
Recall NumberF-0110-2013

Class I Food Event

Event ID63193
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date15-Sep-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmCaito Foods Service, Inc.
CityIndianapolis
StateIN
CountryUS
Distribution Pattern4 Distributors in WI, IN, IL, CA with further nationwide distribution to retail stores
 

Associated Products

Product DescriptionNice, Fruit Mango, Product of Mexico, single, 6 ct; UPC 0.4902252988.5
Code InfoItem Number 381030, Best By 8/04/12 -09/14/12
ClassificationClass I
Reason for RecallIn 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 Quantity497
Recall NumberF-0127-2013
Product DescriptiondeLISH, 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 InfoSpears:Item 383138; Best By 8/04/12 -09/14/12 Medey :item 383137; Best By 8/04/12 -09/14/12
ClassificationClass I
Reason for RecallIn 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 Quantity2633 cases medley, 2137 cases spears
Recall NumberF-0128-2013
Product DescriptionDeLish, 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 InfoDeLish 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
ClassificationClass I
Reason for RecallIn 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 Quantityall types 16,297 cases
Recall NumberF-0129-2013
Product DescriptiondeLISH, 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 InfoItem 383827; Best By 8/04/2012- 09/16/12
ClassificationClass I
Reason for RecallIn 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 Quantity1062 cases
Recall NumberF-0130-2013
Product DescriptionGarden 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 InfoGarden 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
ClassificationClass I
Reason for RecallIn 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 Quantity14,711
Recall NumberF-0131-2013
Product DescriptionTropical 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 InfoGarden Highway Item 383006 Trader Joes item 383088 deLish item 383137 Best By 8/04/2012- 09/16/12
ClassificationClass I
Reason for RecallIn 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 Quantity3930
Recall NumberF-0132-2013
Product DescriptionGarden 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 InfoItem 382987, Best By 8/04/2012- 09/16/12
ClassificationClass I
Reason for RecallIn 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 Quantity7 cases
Recall NumberF-0133-2013
Product DescriptionGarden 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 InfoItem 382986, Best By 8/04/2012- 09/16/12
ClassificationClass I
Reason for RecallIn 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 NumberF-0134-2013
Product DescriptionGarden Highway,Watermelon Mango Medley, Net Wt 7oz, UPC 8.26766-24062.3, Ingredients: Watermelon, Mango, Blueberries in its Own Juice
Code InfoItem 383106, Best By 7/26/2012- 09/09/12
ClassificationClass I
Reason for RecallIn 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 Quantity2 cases
Recall NumberF-0135-2013
Product DescriptionFruit 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 InfoItem 383009, Best By 8/04/2012- 09/16/12
ClassificationClass I
Reason for RecallIn 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 NumberF-0136-2013
Product DescriptionSeasonal 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 InfoItem 383334 and 383477, Best if Sold by 8/04/2012- 09/16/12
ClassificationClass I
Reason for RecallIn 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 Quantity8582
Recall NumberF-0137-2013
Product DescriptionSignature Cafe Fruit Basket Medley 30 oz (1 lb 14 oz), UPC 8.26766-06918, Ingredients Grapes,Pineapple, Cantaloupe, Mango, Watermelon, apples
Code InfoItem 383062, Use By SEP 1612
ClassificationClass I
Reason for RecallIn 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 Quantity674
Recall NumberF-0138-2013

Class I Food Event

Event ID63213
StatusTerminated
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date17-Sep-12
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmLiberty Fruit Co Inc - Carols Cuts Div
CityKansas City
StateKS
CountryUS
Distribution PatternDistribution was made to KS.
 

Associated Products

Product DescriptionCarol'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 InfoLot number 81260-1824, use by date 9/2/2012
ClassificationClass I
Reason for RecallProduct is potentially contaminated with Salmonella gaminara.
Product Quantity185/5-lb trays
Recall NumberF-0111-2013

Class I Food Event

Event ID63217
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date10-Sep-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmFloyd Peterson Company Inc.
CityAuburn
StateWA
CountryUS
Distribution PatternProduct distributed to distributors, retailers, and restaurants in Oregon and Washington.
 

Associated Products

Product DescriptionRicotta 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 MARTE***IMPORTED BY FOREVER CHEESE,NY 11106***PRODUCT OF ITALY***"
Code Infomanufacturer codes 7022, 7212, 7272 and 7432.
ClassificationClass I
Reason for RecallRicotta Salata Frescolina Brand Cheese is recalled due to the potential contamination with Listeria monocytonenes.
Product Quantitytotal 390 lbs
Recall NumberF-0122-2013

Class I Food Event

Event ID63269
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date13-Sep-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmSpecialty Commodities, Inc.
CityFargo
StateND
CountryUS
Distribution PatternCA, GA, IL, MO, NY, TX, WA
 

Associated Products

Product DescriptionMacadamia Nuts Style 2, RAW, SHELLED. DESCRIPTION OF CARTON FROM GUATEMALA: LOT 2 70 JUNE 25/12 423, 43 1 NORMAL/BIG .
Code InfoLot #: 275 & 271 BEST BEFORE MAY/14, 1427
ClassificationClass I
Reason for RecallSpecialty Commodities Inc., is recalling product due to potential contamination with Salmonella.
Product Quantity27,350 lbs (1094- 25 lb cartons)
Recall NumberF-0124-2013

Class I Food Event

Event ID63274
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date18-Sep-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmWorld Food LLC.
CityOrlando
StateFL
CountryUS
Distribution PatternDistributed throughout FL.
 

Associated Products

Product DescriptionFresh Fruit Burst fruit cup, packaged in 1 and 1.5 lb containers. Labeled in part: "***Fruit Burst***Ingredients: Watermelon, Cantaloupe, Pineapple, Honeydew, Grapes, Mango, Blueberries. Packed in its own juice***"
Code InfoWorld 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
ClassificationClass I
Reason for RecallOn 09/18/2012, World Foods, LLC recalled various products containing mangoes supplied from Agricola Daniella with the potential to be contaminated with Salmonella.
Product Quantity7220 lbs/1455 cases
Recall NumberF-0148-2013
Product Description Mango Spears, packaged in 1 lb containers. Labeled in part: "***Mango Spears***Ingredients: Mango***Packed in its own juice***Grown in: Mexico ***"
Code InfoWorld Food Lot Code 011347 Best if Sold By: 09/21/2012, 09/22/2012, UPC Code 21140-01694
ClassificationClass I
Reason for RecallOn 09/18/2012, World Foods, LLC recalled various products containing mangoes supplied from Agricola Daniella with the potential to be contaminated with Salmonella.
Product Quantity244 lbs/ 61 cases
Recall NumberF-0149-2013
Product DescriptionFresh Island Medley, packaged in 1 lb containers. Labeled in part: "***Island Medley***Ingredients: Pineapple, Mango, Papaya***Packed in its own juice****"
Code InfoWorld Food Lot Code 011347 Best if Sold By: 09/13/2012, 09/21/2012, 09/22/2012, 09/23/2012 UPC Code 21140-01696
ClassificationClass I
Reason for RecallOn 09/18/2012, World Foods, LLC recalled various products containing mangoes supplied from Agricola Daniella with the potential to be contaminated with Salmonella.
Product Quantity700lbs/175 cases
Recall NumberF-0150-2013

Class I Food Event

Event ID63289
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date25-Sep-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmPublix Super Markets
CityLakeland
StateFL
CountryUS
Distribution PatternFlorida, Georgia, South Carolina, Alabama, and Tennessee
 

Associated Products

Product Description***Publix***Hearts of Romaine***Chopped Hearts of Romaine***Triple Washed***& Ready to Eat***No Preservatives***NET WT 10 OZ (284g)***
Code InfoBest if used by Sept 20
ClassificationClass I
Reason for RecallListeria Monocytogenes in a sample collected by IEH and confirmed by FDA
Product Quantity763 cases
Recall NumberF-0108-2013

Class I Food Event

Event ID63298
StatusTerminated
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date26-Sep-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmGretchen's Shoebox Express
CitySeattle
StateWA
CountryUS
Distribution PatternProduct was distributed to retail stores in Washington.
 

Associated Products

Product DescriptionEvolution 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 InfoEnjoy by: 9/24/12, 9/25/12
ClassificationClass I
Reason for RecallThe almond butter used to manufacture the product, supplied by Sunland, Inc., is potentially contaminated with Salmonella.
Product Quantity12 units
Recall NumberF-0125-2013
Product DescriptionEvolution 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 InfoEnjoy by: 9/25/12, 9/26/12, 10/2/12, 10/3/12, 10/7/12
ClassificationClass I
Reason for RecallThe almond butter used to manufacture the product, supplied by Sunland, Inc., is potentially contaminated with Salmonella.
Product Quantity8 units
Recall NumberF-0126-2013

Class I Food Event

Event ID63318
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date28-Sep-12
Initial Firm Notification of Consignee or Public E-Mail
Recalling FirmC.G. Higgins Confections, LLC
CitySanta Fe
StateNM
CountryUS
Distribution PatternRetailers and end users located in NM, USA.
 

Associated Products

Product DescriptionPeanut Butter Fudge 3 oz bag, manufactured from 6-28-12 thru 9-20-12
Code InfoNo manufacturing code.
ClassificationClass I
Reason for RecallPeanut Butter used to product Peanut Butter Fudge was recalled by Sunland, Inc.; therefore, this product has the potential to be contaminated with Salmonella.
Product Quantity132 lbs
Recall NumberF-0140-2013

Class I Food Event

Event ID63320
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date27-Sep-12
Initial Firm Notification of Consignee or Public E-Mail
Recalling FirmNewman's Own Organics
CityAptos
StateCA
CountryUS
Distribution PatternThe 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 DescriptionNewman'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 InfoExpiration Dates: 11/26/10 and later
ClassificationClass I
Reason for RecallThe product was manufactured using peanut butter recalled by Sunland Inc. and it may be contaminated with Salmonella.
Product Quantity4,609 cases or 27,654 packages total
Recall NumberF-0292-2013

Class I Food Event

Event ID63339
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date02-Oct-12
Initial Firm Notification of Consignee or Public E-Mail
Recalling FirmWhole Foods Market Group Inc.
CityEverett
StateMA
CountryUS
Distribution PatternMassachusetts, Rhode Island, Maine, Connecticut, New York and New Jersey
 

Associated Products

Product DescriptionWhole Foods Roasted Garlic Eggplant Soup , 24oz plastic container UPC: 3640630269
Code InfoSell By: October 14 2012
ClassificationClass I
Reason for RecallProduct labeled as Whole Foods Roasted Garlic and Eggplant Soup may contain Lobster Corn Bisque. Undeclared allergens: Shellfish, Milk
Product Quantity360/24 oz
Recall NumberF-0290-2013

Class I Food Event

Event ID63340
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date02-Oct-12
Initial Firm Notification of Consignee or Public Press Release
Recalling FirmGretchen's Shoebox Express
CitySeattle
StateWA
CountryUS
Distribution PatternProduct was distributed at cafe stores in Oregon and Washington only. There are no Canadian consignees.
 

Associated Products

Product DescriptionStarbuck 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 InfoEnjoy 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.
ClassificationClass I
Reason for RecallThe 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 Quantityapproximately 16, 752 units
Recall NumberF-0139-2013

Class I Food Event

Event ID63342
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date28-Sep-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmLate July Snacks, LLC
CityBarnstable
StateMA
CountryUS
Distribution PatternNationwide
 

Associated Products

Product DescriptionLate 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 Info5 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)
ClassificationClass I
Reason for RecallOrganic Mini Peanut Butter Sandwich Crackers are recalled due to Sunland peanut butter recall due to the potential to be contaminated with Salmonella
Product Quantity12,681 cases
Recall NumberF-0291-2013

Class I Food Event

Event ID63388
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date05-Oct-12
Initial Firm Notification of Consignee or Public Press Release
Recalling FirmKilwin's Quality Confections, Inc.
CityPetoskey
StateMI
CountryUS
Distribution PatternMichigan 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 DescriptionKilwins Sugar Free S/F PEANUT BUTTER FUDGE, Nt. Wt. 7-oz (198 g)
Code InfoItem 648, bar code 000648, lots 67936, 67105, 66959, 66413, 66248, 65123, 63124, 62693, 62612, 61658, 61621
ClassificationClass I
Reason for RecallThe 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 Quantity640 pkgs (160 four count cases)
Recall NumberF-0141-2013

Class II Biologics Event

Event ID40327
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date28-Dec-04
Initial Firm Notification of Consignee or Public FAX
Recalling FirmOgden Medical Center, Inc.
CityOgden
StateUT
CountryUS
Distribution PatternUT, Switzerland
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code Info7060020
ClassificationClass II
Reason for RecallBlood products, which were collected from a donor who traveled to a malarial endemic area, were distributed.
Product Quantity1 unit
Recall NumberB-2422-12

Class II Biologics Event

Event ID40858
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date11-Oct-05
Initial Firm Notification of Consignee or Public FAX
Recalling FirmPoudre Valley Health Care, Inc
CityFort Collins
StateCO
CountryUS
Distribution PatternCO, NJ
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code Info8623753; 8624162
ClassificationClass II
Reason for RecallBlood products, which were collected from a donor who traveled to malarial endemic areas, were distributed.
Product Quantity2 units
Recall NumberB-2417-12

Class II Biologics Event

Event ID40965
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date02-Nov-05
Initial Firm Notification of Consignee or Public FAX
Recalling FirmPoudre Valley Health Care, Inc
CityFort Collins
StateCO
CountryUS
Distribution PatternCO, NJ
 

Associated Products

Product DescriptionFresh Frozen Plasma
Code Info8623581
ClassificationClass II
Reason for RecallBlood products, collected from a donor whose arm scrub may have been incorrectly performed, was distributed.
Product Quantity1 unit
Recall NumberB-2428-12

Class II Biologics Event

Event ID42336
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date19-May-06
Initial Firm Notification of Consignee or Public Letter
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternMO, CA.
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW045006028414
ClassificationClass II
Reason for RecallBlood products, which were collected from a donor who traveled to a malarial endemic area, were distributed.
Product Quantity1 Unit
Recall NumberB-2443-12

Class II Biologics Event

Event ID47615
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date07-Feb-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternMissouri
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW045008901224 (Part A); W045008901224(Part B)
ClassificationClass II
Reason for RecallBlood products, with positive bacterial detection testing, were distributed.
Product Quantity2 Units
Recall NumberB-2456-12

Class II Biologics Event

Event ID47616
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date11-Feb-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternKansas
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW045008901655(Part A); W045008901655(Part B)
ClassificationClass II
Reason for RecallBlood Products, which were contaminated with Aspergillus versicolor, were distributed.
Product Quantity2 Units
Recall NumberB-2511-12

Class II Biologics Event

Event ID47617
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date27-Feb-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternKansas; Missouri
 

Associated Products

Product DescriptionFresh Frozen Plasma
Code InfoW045008902885
ClassificationClass II
Reason for RecallBlood Products, which were contaminated with Aspergillus versicolor, were distributed.
Product Quantity1 Unit
Recall NumberB-2512-12
Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW045008902885
ClassificationClass II
Reason for RecallBlood Products, which were contaminated with Aspergillus versicolor, were distributed.
Product Quantity1 Unit
Recall NumberB-2513-12

Class II Biologics Event

Event ID47619
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date22-Feb-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternMissouri; Kansas
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW045008902809
ClassificationClass II
Reason for RecallBlood products, which were possibly contaminated with Propionibacterium species, were distributed.
Product Quantity1 Unit
Recall NumberB-2508-12
Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW045008902809
ClassificationClass II
Reason for RecallBlood products, which were possibly contaminated with Propionibacterium species, were distributed.
Product Quantity1 Unit
Recall NumberB-2509-12

Class II Biologics Event

Event ID47981
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date25-Mar-08
Initial Firm Notification of Consignee or Public FAX
Recalling FirmCommunity Blood Bank of Lancaster County Medical Society
CityLincoln
StateNE
CountryUS
Distribution PatternNE; Austria
 

Associated Products

Product DescriptionBlood and Blood Products for Reprocessing
Code Info9128014
ClassificationClass II
Reason for RecallBlood products, collected from a donor with a history of Hepatitis A, were distributed.
Product Quantity1 unit
Recall NumberB-2415-12
Product DescriptionRed Blood Cells Leukocytes Reduced
Code Info9128014
ClassificationClass II
Reason for RecallBlood products, collected from a donor with a history of Hepatitis A, were distributed.
Product Quantity1 unit
Recall NumberB-2416-12

Class II Biologics Event

Event ID47984
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date18-Feb-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternMissouri
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced Irradiated
Code InfoW045008900034
ClassificationClass II
Reason for RecallBlood products, which did not meet the acceptable product specifications for release, was distributed.
Product Quantity1 Unit
Recall NumberB-2427-12

Class II Biologics Event

Event ID49294
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date03-Jul-08
Initial Firm Notification of Consignee or Public Letter
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternMissouri
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW045007086237
ClassificationClass II
Reason for RecallBlood products, collected from a donor who was illiterate, were distributed.
Product Quantity1 Unit
Recall NumberB-2446-12
Product DescriptionFresh Frozen Plasma
Code InfoW045007086237
ClassificationClass II
Reason for RecallBlood products, collected from a donor who was illiterate, were distributed.
Product Quantity1 Unit
Recall NumberB-2447-12

Class II Biologics Event

Event ID49353
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date15-Jul-08
Initial Firm Notification of Consignee or Public Letter
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternMO
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW045008039993
ClassificationClass II
Reason for RecallBlood product, collected from a donor whose health history screening was inadequately performed, was distributed.
Product Quantity1 Unit
Recall NumberB-2448-12

Class II Biologics Event

Event ID50605
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date23-Oct-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmAmerican National Red Cross (The)
CityDedham
StateMA
CountryUS
Distribution PatternMA
 

Associated Products

Product DescriptionRed Blood Cells (Apheresis) Leukocytes Reduced
Code Info004GE05195P1;004GE05195P2
ClassificationClass II
Reason for RecallBlood products, requiring testing for separator validation, were distributed without testing.
Product Quantity2 units
Recall NumberB-2408-12

Class II Food Event

Event ID61291
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date17-Feb-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmSunshine Peanut Company
CityJacksonville
StateFL
CountryUS
Distribution PatternProduct was distributed to distributors in CA, FL, NJ, and WA.
 

Associated Products

Product DescriptionSunny 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 PEANUTS***Sunshine Peanut Company Tampa, FL 33637*** -- Driscoll product 1,344 cases Lot 111912 & 112012. 35 lb pail labeled in part: ""SunnyBoy Creamy PEANUT BUTTER***Net 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 PEANUTS***Sunshine Peanut Company Tampa, FL 33637*** -- South Bay Correctional Facility, South Bay, FL (Good Source) 72 Pails Lot 112412.
Code Infolot codes: 111912, 112012, 112412.
ClassificationClass II
Reason for RecallOn 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 Quantity72 - 35lb pails; 1344 - 6/5lb Tubs.
Recall NumberF-0113-2013
Product DescriptionSunny Boy Low Sodium/ Low Salt Peanut Butter. Product is labeled in part: 35 lb pail labeled in part: ""SunnyBoy LowSodium/LowSalt***PEANUT BUTTER***Net 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 PEANUTS***Sunshine Peanut Company Tampa, FL 33637*** US Food Service, Boca Raton, FL Lot 113012 Qty 846 pails.
Code Infolot codes: 112312.
ClassificationClass II
Reason for RecallOn 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 Quantity846 pails
Recall NumberF-0114-2013
Product DescriptionSunny Boy NoSalt Peanut Butter. No label was provided by the firm for this product. Product would have been labeled in part: "***SunnyBoy CREAMY PEANUT BUTTER***Net Wt. 35lb. (15.89KG)***Product of USA***" Marion C.I. (US Food)Lot 112012 - 12 Pails shipped.
Code Infolot code: 112012
ClassificationClass II
Reason for RecallOn 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 Quantity12 pails
Recall NumberF-0115-2013
Product DescriptionProduct 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 Peanuts***Sunshine Peanut Company Jacksonville, FL 32204***SP767***" Case label - "200/1oz PEANUT BUTTER***PRODUCT 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 Infolot code: 112312
ClassificationClass II
Reason for RecallOn 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 NumberF-0116-2013
Product DescriptionProduct 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 Peanuts***Sunshine Peanut Company Jacksonville, FL 32204***SP767***" Case Label: "***200/ 2oz Pouch***PEANUT BUTTER***SUNSHINE PEANUT CO.***JACKSONVILLE, FL. 32204***" -- 200/2oz Lot 112312, 112412, 120112 406 shipped to Harvest Farms, Lancaster, CA.
Code Infolot code: 112312, 112412, 120112.
ClassificationClass II
Reason for RecallOn 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 Quantity406 cases
Recall NumberF-0117-2013
Product DescriptionProduct is 50 lb Bag Peanut Butter. Product Case is labeled in part: "***50 Lbs Bag***PEANUT BUTTER***PRODUCT 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 BUTTER***PRODUCT OF USA***" 10 / 5 Lb Bags Lot 113112 - 48 boxes shipped to Cheney Brothers, Ocala, FL.
Code Infolot code: 113112.
ClassificationClass II
Reason for RecallOn 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 Quantity48 boxes (10/5 Lb Bags) & 225 boxes (50 Lb Bags)
Recall NumberF-0118-2013

Class II Food Event

Event ID62280
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date04-Jun-12
Initial Firm Notification of Consignee or Public Visit
Recalling FirmSun Boricua Pa'l Mundo Inc.
CityCamuy
StatePR
CountryUS
Distribution PatternPuerto 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 Info6-3-13, 2-4-13, 3-4-13, 13-4-13, 2-5-13, 1-6-13
ClassificationClass II
Reason for RecallUndeclared color additives: FD&C Yellow #5, Yellow #6 and Red #40.
Product Quantity36,000 units
Recall NumberF-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 Info6-3-13, 7-3-13, 16-3-13, 28-3-13, 2-4-13, 3-4-13, 1-5-13, 28-5-13
ClassificationClass II
Reason for RecallUndeclared color additives: FD&C Yellow #5, Yellow #6 and Red #40.
Product Quantity48,000 units
Recall NumberF-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 Info3-3-13, 5-3-13, 6-3-13, 1-5-13, 2-5-13, 1-6-13
ClassificationClass II
Reason for RecallUndeclared color additives: FD&C Yellow #5, Yellow #6 and Red #40.
Product Quantity36,000 units
Recall NumberF-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 Info3-3-13, 7-3-13, 16-3-13, 29-3-13, 3-4-13, 4-4-13, 1-5-13, 2-5-13, 1-6-12
ClassificationClass II
Reason for RecallUndeclared color additives: FD&C Yellow #5, Yellow #6 and Red #40.
Product Quantity
Recall NumberF-0296-2013

Class II Devices Event

Event ID62569
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date20-Apr-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmOsteotech Inc
CityEatontown
StateNJ
CountryUS
Distribution PatternWorldwide Distribution - USA (nationwide) and Internationally.
 

Associated Products

Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0083-2013
Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0084-2013
Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0085-2013
Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0086-2013
Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0087-2013
Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0088-2013
Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0089-2013
Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0090-2013
Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0091-2013
Product DescriptionGrafton 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0092-2013
Product DescriptionOptimum 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0093-2013
Product DescriptionOptimum 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 Info510 K042707; K043048; K051188; K051195 Multiple Lots - please see attachment
ClassificationClass II
Reason for RecallMultiple 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 Quantity79,207 units for all products in recall event
Recall NumberZ-0094-2013

Class II Biologics Event

Event ID62584
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date06-Jul-12
Initial Firm Notification of Consignee or Public FAX
Recalling FirmBlood Assurance Inc
CityChattanooga
StateTN
CountryUS
Distribution PatternTennessee; North Carolina; Indiana
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW043212020538; W043211042995;
ClassificationClass II
Reason for RecallBlood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
Product Quantity2
Recall NumberB-2304-12
Product DescriptionBlood and Blood Products for Reprocessing
Code InfoW043212020538; W043211042995;
ClassificationClass II
Reason for RecallBlood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
Product Quantity2
Recall NumberB-2305-12

Class II Biologics Event

Event ID62602
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date06-Jul-12
Initial Firm Notification of Consignee or Public FAX
Recalling FirmOur Lady Of The Lake Hospital Inc
CityBaton Rouge
StateLA
CountryUS
Distribution PatternLouisiana
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW165712013005R;
ClassificationClass II
Reason for RecallBlood product, collected from a donor who reported travel to an area possibly endemic for malaria, was distributed.
Product Quantity1
Recall NumberB-2374-12

Class II Biologics Event

Event ID62620
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date31-May-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmHCSC-Blood Center
CityBethlehem
StatePA
CountryUS
Distribution PatternPennsylvania
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced Irradiated
Code InfoW050912011533;
ClassificationClass II
Reason for RecallBlood products, collected from a donor whose medical history screening was incomplete, were distributed.
Product Quantity1
Recall NumberB-2376-12
Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW050912011533;
ClassificationClass II
Reason for RecallBlood products, collected from a donor whose medical history screening was incomplete, were distributed.
Product Quantity1
Recall NumberB-2377-12

Class II Biologics Event

Event ID62630
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date21-Jun-12
Initial Firm Notification of Consignee or Public FAX
Recalling FirmLifeSouth Community Blood Centers, Inc.
CityGainesville
StateFL
CountryUS
Distribution PatternAlabama
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW115112181422P; W115112181422P (split product)
ClassificationClass II
Reason for RecallBlood products, labeled leukoreduced without assurance that they met the criteria for leukoreduced products, were distributed
Product Quantity2
Recall NumberB-2378-12

Class II Biologics Event

Event ID62632
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date13-Jun-12
Initial Firm Notification of Consignee or Public FAX
Recalling FirmLifeSouth Community Blood Centers Inc - Birmingham Region
CityBirmingham
StateAL
CountryUS
Distribution PatternAlabama
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW1151121927911;
ClassificationClass II
Reason for RecallBlood product, with platelet count below the specified minimum requirement, was distributed.
Product Quantity1
Recall NumberB-2380-12

Class II Biologics Event

Event ID62633
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date11-Jun-12
Initial Firm Notification of Consignee or Public FAX
Recalling FirmLifeSouth Community Blood Centers Inc - Birmingham Region
CityBirmingham
StateAL
CountryUS
Distribution PatternAlabama
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW115112192067K;
ClassificationClass II
Reason for RecallBlood product, with platelet count below the specified minimum requirement, was distributed.
Product Quantity1
Recall NumberB-2381-12

Class II Biologics Event

Event ID62634
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date13-Jun-12
Initial Firm Notification of Consignee or Public FAX
Recalling FirmLifeSouth Community Blood Centers Inc - Birmingham Region
CityBirmingham
StateAL
CountryUS
Distribution PatternAlabama
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW115112192059K;
ClassificationClass II
Reason for RecallBlood product, with platelet count below the specified minimum requirement, was distributed.
Product Quantity1
Recall NumberB-2382-12

Class II Biologics Event

Event ID62739
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date26-Jun-12
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmTri-counties Blood Bank
CitySan Luis Obispo
StateCA
CountryUS
Distribution PatternCalifornia
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced Irradiated
Code InfoW1428124064601 Part 1; W1428124064601 Part 2;
ClassificationClass II
Reason for RecallBlood products, which were labeled as leukoreduced, but were not tested to verify the White Blood Cell count, were distributed.
Product Quantity2
Recall NumberB-2477-12

Class II Biologics Event

Event ID62742
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date11-Jul-12
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center of Carolinas
CityCharlotte
StateNC
CountryUS
Distribution PatternNorth Carolina
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW227012003998 Part 1 ; W227012003998 PART 2;
ClassificationClass II
Reason for RecallBlood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity2
Recall NumberB-2482-12

Class II Biologics Event

Event ID62808
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date21-Jun-12
Initial Firm Notification of Consignee or Public FAX
Recalling FirmLifeSouth Community Blood Centers, Inc.
CityDunwoody
StateGA
CountryUS
Distribution PatternGeorgia
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW115112199093F;
ClassificationClass II
Reason for RecallBlood products, which were labeled as leukoreduced, but were not tested to verify the White Blood Cell count, were distributed.
Product Quantity1
Recall NumberB-2485-12

Class II Biologics Event

Event ID62809
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date18-Apr-12
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmBlood Systems, Inc.
CityReno
StateNV
CountryUS
Distribution PatternNevada, Arizona, Mississippi
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code InfoW041911037651K; WO419110435677; W041912003080G; W0419120020419; W041912002091Q; W041911040658C;
ClassificationClass II
Reason for RecallBlood products, with insufficient plasma volume to support the platelet yield, were distributed.
Product Quantity6
Recall NumberB-2486-12

Class II Food Event

Event ID62831
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date07-Aug-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmErnesto Tropical Food, Inc
CityPonce
StatePR
CountryUS
Distribution PatternPuerto Rico only (distributors and retailers in the local area)
 

Associated Products

Product Description"Sofrito a Mi Gusto***100% Natural (Natural Seasoning)***Keep Refrigerated***Elaborado y Envasado por Ernesto Tropical Foods, Inc. Guadalupe#62 Ponce, Puerto Rico 00731***"
Code InfoTBD
ClassificationClass II
Reason for RecallUndeclared allergens: FD&C Yellow #5
Product Quantity576 units
Recall NumberF-0142-2013
Product Description"Recaito Doña Tita***Home Made Style***Keep Refrigerated***Elaborado y Envasado por Ernesto Tropical Foods, Inc. Guadalupe #62, Ponce PR 00731***Net Weight: 14 oz***"
Code Info5774, 5780, 5783, 5784, 5785, 5803, 5805, 5806, 5824, 5834, 5836, 5840, 5850, 5863, 5868, 5881, 5898, 5903, 5942, 5949, 3966, 5707, 5708, 5709
ClassificationClass II
Reason for RecallUndeclared allergens: FD&C Yellow #5
Product Quantity528 units
Recall NumberF-0143-2013

Class II Devices Event

Event ID63086
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date09-Jan-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmThe Anspach Effort, Inc.
CityPalm Beach Gardens
StateFL
CountryUS
Distribution PatternWorldwide Distribution - US (nationwide) and the countries of: Italy, Japan, Switzerland, Turkey and Taiwan.
 

Associated Products

Product Description"***Electric Systems Foot Control****Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
Code InfoSerial Numbers: E31305311301, E31305311302, E31305311303, E31305311304, E31305311401, E31305311402, E31305311403, E31305311404, E31305311405, E32305311201, E32305311202, E33305311501, E33305311502, E33305311504, and E33305311505
ClassificationClass II
Reason for RecallThe 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 Quantity16 units
Recall NumberZ-0074-2013
Product Description"***Electric Systems Foot Control with Direction Only***Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
Code InfoSerial Numbers: E28305271001, E28305271002, E28305271003, E28305271004, E2830527100, E28305271006, E28305271007, E28305271008, E2830521009, E28305271010, E29305270901, E29305270902, E29305270903, E29305271101, E29305271102, E29305271103, E29305271104, E29305271105, E29305271106, E29305271107, E29,
ClassificationClass II
Reason for RecallThe 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 Quantity41 units
Recall NumberZ-0075-2013
Product Description"***Electric Systems Foot Control with Direction and Irrigation***Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
Code InfoSerial Numbers: E3230327501, E32305327502, E32305327503, E32305327504, E32305327505, E32305327601, E32305327602, E32305327603, E32305327604, and E32305327605
ClassificationClass II
Reason for RecallThe 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 Quantity10 units
Recall NumberZ-0076-2013

Class II Devices Event

Event ID63115
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date26-Jun-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmLinvatec Corp. dba ConMed Linvatec
CityLargo
StateFL
CountryUS
Distribution PatternWorldwide 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"***PressFT***2.6 w/ Two #1 (4 metric) Hi-Fi***Sutures***NP262***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures
Code InfoItem number NP262
ClassificationClass II
Reason for RecallLinvatec 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 Quantity879 units for all products in recall event
Recall NumberZ-0063-2013
Product Description"***PressFT***2.6 w/ One #2 (5 metric) Hi-Fi***Suture***NP261***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures
Code InfoItem number NP261
ClassificationClass II
Reason for RecallLinvatec 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 Quantity879 units for all products in recall event
Recall NumberZ-0064-2013
Product Description"***Press FT***2.6 w/ One #2 (5 metric) Hi-Fi***Suture, HIP***N2***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures
Code InfoItem number NP261H
ClassificationClass II
Reason for RecallLinvatec 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 Quantity879 units for all products in recall event
Recall NumberZ-0065-2013
Product Description"***PressFT***2.1 w/ Two #0 (3.5 metric) Hi-Fi***Sutures***NP212***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures
Code InfoItem number NP212
ClassificationClass II
Reason for RecallLinvatec 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 Quantity879 units for all products in recall event
Recall NumberZ-0066-2013
Product Description"***PressFT***2.1 w/ One #2 (5 metric) Hi-Fi***Suture***NP211***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures
Code InfoItem number NP211
ClassificationClass II
Reason for RecallLinvatec 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 Quantity879 units for all products in recall event
Recall NumberZ-0067-2013
Product DescriptionNP211H***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures
Code InfoItem number NP211H
ClassificationClass II
Reason for RecallLinvatec 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 Quantity879 units for all products in recall event
Recall NumberZ-0068-2013

Class II Devices Event

Event ID63124
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date13-Sep-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmZimmer, Inc.
CityWarsaw
StateIN
CountryUS
Distribution PatternWorldwide 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 DescriptionCPT 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 InfoLot 61947708
ClassificationClass II
Reason for RecallZimmer 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 Quantity59 both units
Recall NumberZ-0060-2013
Product DescriptionCPT 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 InfoLot 62017554
ClassificationClass II
Reason for RecallZimmer 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 Quantity20
Recall NumberZ-0061-2013
Product DescriptionCPT 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
ClassificationClass II
Reason for RecallZimmer 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 Quantity59 both lots
Recall NumberZ-0062-2013

Class II Devices Event

Event ID63155
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date11-Apr-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmBeckman Coulter Inc.
CityBrea
StateCA
CountryUS
Distribution PatternWorldwide 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 DescriptionAutoMate 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 InfoAll Serial Numbers
ClassificationClass II
Reason for RecallThe 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 Quantity468 units total (51 units in US)
Recall NumberZ-0056-2013

Class II Food Event

Event ID63159
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date10-Sep-12
Initial Firm Notification of Consignee or Public E-Mail
Recalling FirmSpartan Central Kitchen
CityGrand Rapids
StateMI
CountryUS
Distribution PatternMI and OH only.
 

Associated Products

Product DescriptionPound Cake 12 ounces
Code InfoAll products with the sell by dates on or before Sept 21st.
ClassificationClass II
Reason for RecallDuring 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 Quantity261
Recall NumberF-0151-2013
Product Description#805 Salad - No Meat Asian 3/4 pounds
Code InfoAll products with the sell by dates on or before September 13.
ClassificationClass II
Reason for RecallDuring 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 Quantity99
Recall NumberF-0152-2013
Product Description#804 Salad - No Meat Chicken Caesar 3/4 pounds
Code InfoAll products with the sell by dates on or before September 13.
ClassificationClass II
Reason for RecallDuring 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 Quantity131
Recall NumberF-0153-2013
Product Description#803 Salad - No Meat 7 Layer 7/8 pounds
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity121
Recall NumberF-0154-2013
Product Description#802 Salad - No Meat Large Chef 3/4 pounds #801 Salad - No Meat Small Chef 1/4 pound
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity1) 141; 2) 132
Recall NumberF-0155-2013
Product Description#767 Salad - Asian Chicken 3/4 pounds
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity437
Recall NumberF-0156-2013
Product Description#766 Salad - Chicken Caesar 3/4 pounds
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity513
Recall NumberF-0157-2013
Product Description#765 Salad - Seven Layer 7/8 pounds
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity678
Recall NumberF-0158-2013
Product Description#764 Salad - Large Chef 3/4 pounds #763 Salad - Small Chef 1/4 pound
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity1) 739; 2) 670
Recall NumberF-0159-2013
Product Description#762 Salad - Large Garden Fresh 3/4 pounds #761 Salad - Small Garden Fresh 3 oz.
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity1) 832; 2) 668
Recall NumberF-0160-2013
Product Description#748 Chicken Spread Sandwich on White each
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity612
Recall NumberF-0161-2013
Product Description#746 Sandwich - Turkey Cheddar each
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity468
Recall NumberF-0162-2013
Product Description#745 Sandwich - Ham & Cheese sandwich
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity443
Recall NumberF-0163-2013
Product Description#744 Sandwich - Sandwich Spread sandwich
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity653
Recall NumberF-0164-2013
Product Description#743 Sandwich - Chicken Spread on Wheat each
Code InfoAll with production dates 8/10/12 to 9/10/12 and UPC 0-11213-89999
ClassificationClass II
Reason for RecallDuring 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 Quantity725
Recall NumberF-0165-2013
Product Description#742 Sandwich - Tuna Spread sandwich
Code InfoAll with production dates 8/10/12 to 9/10/12 and UPC 0-11213-89998
ClassificationClass II
Reason for RecallDuring 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 Quantity686
Recall NumberF-0166-2013
Product Description#741 Sandwich - Egg Salad on Wheat sandwich
Code InfoAll with production dates 8/10/12 to 9/10/12 and UPC 0-11213-90011
ClassificationClass II
Reason for RecallDuring 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 Quantity764
Recall NumberF-0167-2013
Product Description#705 Panini - Rotisserie Chicken sandwich
Code InfoAll with production dates 8/10/12 to 9/10/12 and UPC 705
ClassificationClass II
Reason for RecallDuring 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 Quantity235
Recall NumberF-0168-2013
Product Description#704 Panini - Reuben sandwich
Code InfoAll with production dates 8/10/12 to 9/10/12 and UPC 704
ClassificationClass II
Reason for RecallDuring 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 Quantity215
Recall NumberF-0169-2013
Product Description#703 Panini - Little Italy sandwich
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity305
Recall NumberF-0170-2013
Product Description#702 Panini - American Club sandwich
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity316
Recall NumberF-0171-2013
Product Description#701 Panini - California Turkey sandwich
Code InfoAll products with the sell by dates on or before September 13th.
ClassificationClass II
Reason for RecallDuring 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 Quantity314
Recall NumberF-0172-2013
Product Description#460 10 oz Broccoli Augratin 10 ounces
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity37
Recall NumberF-0173-2013
Product Description#459 12 oz Sour Cream & Chive Redskin Potatoes 12 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity488
Recall NumberF-0174-2013
Product Description#455 12 oz Fried Rice with Pineapple 12 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity292
Recall NumberF-0175-2013
Product Description#451 12 oz Cheezy Potatoes 12 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity702
Recall NumberF-0176-2013
Product Description#450 10 oz Garden Veggies 10 ounces
Code InfoAll products with the sell by dates on or before September 15th.
ClassificationClass II
Reason for RecallDuring 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 Quantity360
Recall NumberF-0177-2013
Product Description#449 10 oz Roasted Corn with Fresh Basil Butter 10 ounces
Code InfoAll products with the sell by dates on or before September 15th.
ClassificationClass II
Reason for RecallDuring 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 Quantity325
Recall NumberF-0178-2013
Product Description#448 10 oz Three Green Veggies 10 ounces
Code InfoAll products witht he sell by dates on or before September 15th.
ClassificationClass II
Reason for RecallDuring 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 Quantity381
Recall NumberF-0179-2013
Product Description#447 2 ct Bacon Twice Bake 12 ounces
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity331
Recall NumberF-0180-2013
Product Description#446 2 ct Triple Cheese Twice Bake 12 ounces
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity406
Recall NumberF-0181-2013
Product Description#445 12 oz Asiago & Artichoke Mashed Potatoes 12 ounces
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity59
Recall NumberF-0182-2013
Product Description#443 10 oz Roasted Potatoes with Dill 10 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity481
Recall NumberF-0183-2013
Product Description#442 10 oz Spinach Artichoke Manicotti 10 ounces
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity343
Recall NumberF-0184-2013
Product Description#441 12 oz Spaghetti in Cherry Tomato Sauce 12 ounces
Code InfoAll products with the sell by dates on or before September 15th.
ClassificationClass II
Reason for RecallDuring 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 Quantity332
Recall NumberF-0185-2013
Product Description#440 12 oz Asparagus Linguini with Lemon Cream 12 ounces
Code InfoAll products with the sell by dates on or before September 15th.
ClassificationClass II
Reason for RecallDuring 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 Quantity440
Recall NumberF-0186-2013
Product Description#439 10 oz Very Green Pasta 12 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity414
Recall NumberF-0187-2013
Product Description#438 10 oz Three Cheese Cheddar & Mac 10 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 NumberF-0188-2013
Product Description#436 10 oz Italian Sausage Penne 10 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity377
Recall NumberF-0189-2013
Product Description#429 10 oz Beef Burrito 10 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity547
Recall NumberF-0190-2013
Product Description#427 10 oz Shepherd's Pie 10 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity951
Recall NumberF-0191-2013
Product Description#426 08 oz Grilled Salmon w/Couscous 8 ounces
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity1407
Recall NumberF-0192-2013
Product Description#425 08 oz Tilapia w/Lemon Orzo
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity1466
Recall NumberF-0193-2013
Product Description#423 12 oz Shredded Chicken Enchilada 12 ounces
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity949
Recall NumberF-0194-2013
Product Description#421 12 oz Chicken Parmesan w/Linguini each
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity992
Recall NumberF-0195-2013
Product Description#416 MME Tilapia No Meat each
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity51
Recall NumberF-0196-2013
Product Description#415 MME Grilled Salmon No Meat each
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity63
Recall NumberF-0197-2013
Product Description#412 MME Coconut Chicken No Meat 8 ounces
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity40
Recall NumberF-0198-2013
Product Description#411 MME Chicken Parmesan No Meat each
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity48
Recall NumberF-0199-2013
Product Description#391 1/2 Roasted Vegetable Quiche 0.5 each
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity74
Recall NumberF-0200-2013
Product Description#390 1/2 Ham Quiche 0.5 each
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity306
Recall NumberF-0201-2013
Product Description#386 1/2 Farmer's Quiche 1/2 each
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity695
Recall NumberF-0202-2013
Product Description#385 1/2 Asparagus Quiche 0.5 each
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity664
Recall NumberF-0203-2013
Product Description#384 1/2 Broccoli Quiche 0.5 each
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity315
Recall NumberF-0204-2013
Product Description#383 2 lb Shredded Chicken Enchilada & Rice 4 each
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity367
Recall NumberF-0205-2013
Product Description#380 2 lb Hearty Mac & Beef 2 pounds
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity294
Recall NumberF-0206-2013
Product Description#373 Nippy Cheese - Pre-Pack 9 ounces
Code InfoAll products with the sell by dates on or before October 2nd.
ClassificationClass II
Reason for RecallDuring 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 Quantity798
Recall NumberF-0207-2013
Product Description#372 Fruit Dip - Pre-Pack 8 ounces
Code InfoAll products with the sell by dates on or before September 29th.
ClassificationClass II
Reason for RecallDuring 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 Quantity517
Recall NumberF-0208-2013
Product Description#371 Taco Layer Dip - 30 oz., #370 Taco Layer Dip, 15 oz.
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity1) 865; 2) 3332
Recall NumberF-0209-2013
Product Description#363 Cheddar Free Ham & Onion Cheeseball 12 ounces
Code InfoAll products with the sell by dates on or before September 22nd.
ClassificationClass II
Reason for RecallDuring 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 Quantity1032
Recall NumberF-0210-2013
Product Description#362 Ham & Onion Cheeseball 12 ounces
Code InfoAll products with the sell by dates on or before September 22nd.
ClassificationClass II
Reason for RecallDuring 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 Quantity4329
Recall NumberF-0211-2013
Product Description#361 VG's Fat Free Caesar Dressing 5 pounds
Code InfoAll products with the sell by dates on or before October 11th.
ClassificationClass II
Reason for RecallDuring 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 Quantity123
Recall NumberF-0212-2013
Product Description#360 VG's Caesar Salad Dressing 5 pounds
Code InfoAll products with the sell by dates on or before October 3rd.
ClassificationClass II
Reason for RecallDuring 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 Quantity375
Recall NumberF-0213-2013
Product Description#358 Savory Seasoning 5 pounds
Code InfoAll products with the sell by dates on or before January 8th.
ClassificationClass II
Reason for RecallDuring 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 Quantity51
Recall NumberF-0214-2013
Product Description#357 Egg Spread 5 pounds
Code InfoAll products with the sell by dates on or before September 15th.
ClassificationClass II
Reason for RecallDuring 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 Quantity65
Recall NumberF-0215-2013
Product Description#356 Tuna Spread 5 pounds
Code InfoAll products with the sell by dates on or before September 15th.
ClassificationClass II
Reason for RecallDuring 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 Quantity14
Recall NumberF-0216-2013
Product Description#354 Bacon Potato - 8 count Pan 8 each
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity128
Recall NumberF-0217-2013
Product Description#353 Triple Cheese Potato - 8 count Pan 8 each
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity161
Recall NumberF-0218-2013
Product Description#347 Sandwich Spread 5 pounds
Code InfoAll products with the sell by dates on or before October 2nd.
ClassificationClass II
Reason for RecallDuring 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 Quantity377
Recall NumberF-0219-2013
Product Description#350 Olive Oil
Code InfoAll with production dates 8/10/12 to 9/10/12
ClassificationClass II
Reason for RecallDuring 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 Quantity25
Recall NumberF-0220-2013
Product Description#346 Mexicana Dip 5 pounds
Code InfoAll products with the sell by date on or before October 11th.
ClassificationClass II
Reason for RecallDuring 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 Quantity351
Recall NumberF-0221-2013
Product Description#345 Chili Con Queso Dip 5 pounds
Code InfoAll products with the sell by dates on or before October 2nd.
ClassificationClass II
Reason for RecallDuring 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 Quantity656
Recall NumberF-0222-2013
Product Description#343 Dill Dip 5 pounds
Code InfoAll products with the sell by dates on or before October 10th.
ClassificationClass II
Reason for RecallDuring 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 Quantity363
Recall NumberF-0223-2013
Product Description#342 Vegetable Dip 5 pounds
Code InfoAll products with the sell by dates on or before October 10th.
ClassificationClass II
Reason for RecallDuring 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 Quantity128
Recall NumberF-0224-2013
Product Description#341 Spinach Dip 5 pounds
Code InfoAll products with the sell by dates on or before October 2nd.
ClassificationClass II
Reason for RecallDuring 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 Quantity1014
Recall NumberF-0225-2013
Product Description#340 Mashed Potatoes 5 pounds
Code InfoAll products with the sell by dates on or before September 21st.
ClassificationClass II
Reason for RecallDuring 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 Quantity957
Recall NumberF-0226-2013
Product Description#338 Tortellini Primavera 5 pounds
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity93
Recall NumberF-0227-2013
Product Description#337 Smoked Mozzerella Salad 5 pounds
Code InfoAll products with the sell by dates on or before September 16th.
ClassificationClass II
Reason for RecallDuring 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 Quantity143
Recall NumberF-0228-2013
Product Description#336 Spaghetti Salad 5 pounds
Code InfoAll products with the sell by dates on or before September 25th.
ClassificationClass II
Reason for RecallDuring 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 Quantity733
Recall NumberF-0229-2013
Product Description#335 Sunshine Salad 5 pounds
Code InfoAll products with the sell by date on or before October 2nd.
ClassificationClass II
Reason for RecallDuring 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 Quantity274
Recall NumberF-0230-2013
Product Description#334 Ambrosia Salad 5 pounds
Code InfoAll products with the sell by date on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity170
Recall NumberF-0231-2013
Product Description#333 Caribbean Fruit Salad 5 pounds
Code InfoAll products with the sell by date on or before October 2nd.
ClassificationClass II
Reason for RecallDuring 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 Quantity203
Recall NumberF-0232-2013
Product Description#332 Tuna Noodle Salad 5 pounds
Code InfoAll products with the sell by dates on or before September 17th.
ClassificationClass II
Reason for RecallDuring 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 Quantity347
Recall NumberF-0233-2013
Product Description#331 Italian Rotini Salad 5 pounds
Code InfoAll with sell by dates on or before 25-Sept with UPC 331
ClassificationClass II
Reason for RecallDuring 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 Quantity143
Recall NumberF-0234-2013
Product Description#330 Neptune Salad 5 pounds
Code InfoAll with sell by dates on or before 17-Sept with UPC 330
ClassificationClass II
Reason for RecallDuring 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 Quantity378
Recall NumberF-0235-2013
Product Description#329 Three Bean Salad 5 pounds
Code InfoAll with sell by dates on or before 2-Oct with UPC 329
ClassificationClass II
Reason for RecallDuring 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 Quantity382
Recall NumberF-0236-2013
Product Description#328 Kay Macaroni Salad 5 pounds
Code InfoAll with sell by dates on or before 29-Sept with UPC 328
ClassificationClass II
Reason for RecallDuring 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 Quantity445
Recall NumberF-0237-2013
Product Description#327 Kay Potato Salad 5 pounds
Code InfoAll with sell by dates on or before 1-Oct with UPC 327
ClassificationClass II
Reason for RecallDuring 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 Quantity477
Recall NumberF-0238-2013
Product Description#326 Pot Pie Mix 5 pounds
Code InfoAll with sell by dates on or before 16-Sept with UPC 326
ClassificationClass II
Reason for RecallDuring 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 Quantity951
Recall NumberF-0239-2013
Product Description#324 Baked Beans 5 pounds
Code InfoAll with sell by dates on or before 2-Oct with UPC 324
ClassificationClass II
Reason for RecallDuring 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 Quantity322
Recall NumberF-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
ClassificationClass II
Reason for RecallDuring 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 Quantity428
Recall NumberF-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
ClassificationClass II
Reason for RecallDuring 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 Quantity381
Recall NumberF-0242-2013
Product Description#320 Mediterranean Orzo Salad 320 5 pounds
Code InfoAll with sell by dates on or before 17-Sep with UPC 320
ClassificationClass II
Reason for RecallDuring 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 Quantity168
Recall NumberF-0243-2013
Product Description#319 Cherry Chicken Penne Salad 319 5 pounds
Code InfoAll with sell by dates on or before 18-Sep with UPC 319
ClassificationClass II
Reason for RecallDuring 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 Quantity155
Recall NumberF-0244-2013
Product Description#318 Grilled Chicken Pasta Salad 318 5 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 318
ClassificationClass II
Reason for RecallDuring 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 Quantity316
Recall NumberF-0245-2013
Product Description#317 Ham & Cheese Salad 317 5 pounds
Code InfoAll with sell by dates on or before 17-Sep with UPC 317
ClassificationClass II
Reason for RecallDuring 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 Quantity482
Recall NumberF-0246-2013
Product Description#315 Greek Feta Pasta Salad 315 5 pounds
Code InfoAll with sell by dates on or before 17-Sep with UPC 315
ClassificationClass II
Reason for RecallDuring 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 Quantity377
Recall NumberF-0247-2013
Product Description#312 Seafood Pasta Salad 312 5 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 312
ClassificationClass II
Reason for RecallDuring 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 Quantity79
Recall NumberF-0248-2013
Product Description#314 Parmesan Roasted Turkey Salad 314 5 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 314
ClassificationClass II
Reason for RecallDuring 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 Quantity105
Recall NumberF-0249-2013
Product Description#311 Fruit & Nut Wild Rice Salad 311 5 pounds
Code InfoAll with sell by dates on or before 16-Sep with UPC 311
ClassificationClass II
Reason for RecallDuring 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 Quantity37
Recall NumberF-0250-2013
Product Description#309 Macaroni Salad, Old Fashioned 309 5 pounds
Code InfoAll with sell by dates on or before 17-Sep UPC 309
ClassificationClass II
Reason for RecallDuring 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 Quantity454
Recall NumberF-0251-2013
Product Description#308 Sour Cream Mac & Cheddar 308 5 pounds
Code InfoAll with sell by dates on or before 17-Sep with UPC 308
ClassificationClass II
Reason for RecallDuring 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 Quantity659
Recall NumberF-0252-2013
Product Description#306 Asian Style Cole Slaw 306 5 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 306
ClassificationClass II
Reason for RecallDuring 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 Quantity204
Recall NumberF-0253-2013
Product Description#305 Homemade Cole Slaw 7 pounds
Code InfoAll with sell by dates on or before 17-Sep with UPC 305
ClassificationClass II
Reason for RecallDuring 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 Quantity732
Recall NumberF-0254-2013
Product Description#304 Bacon Cheddar Potato Salad 304 5 pounds
Code InfoAll with sell by dates on or before 17-Sep with UPC 304
ClassificationClass II
Reason for RecallDuring 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 Quantity816
Recall NumberF-0255-2013
Product Description#303 Red White & Bleu Potato Salad 5 pounds
Code InfoAll with sell by dates on or before 16-Sep with UPC 303
ClassificationClass II
Reason for RecallDuring 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 Quantity259
Recall NumberF-0256-2013
Product Description#302 Old Fashioned Potato Salad 302 5 pounds
Code InfoAll with sell by dates on or before 17-Sep with UPC 302
ClassificationClass II
Reason for RecallDuring 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 Quantity1590
Recall NumberF-0257-2013
Product Description#301 Creamy Redskin Potato Salad 5 pounds
Code InfoAll with sell by dates on or before 16-Sep with UPC 301
ClassificationClass II
Reason for RecallDuring 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 Quantity1666
Recall NumberF-0258-2013
Product Description#234 Bulk Watermelon 234 2.5 pounds and #050 Watermelon Tray 16 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 234 and 0-11213-90395
ClassificationClass II
Reason for RecallDuring 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 Quantity48 (Bulk) and 792 (Tray)
Recall NumberF-0259-2013
Product Description#233 Bulk Pineapple Chunks, 3 pounds; #076 Pineapple Chunks Fruit Cup, 9 oz.
Code Infosell by date 9/15/12
ClassificationClass II
Reason for RecallDuring 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 Quantity55
Recall NumberF-0260-2013
Product Description#232 Bulk Honeydew 232 3 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 232
ClassificationClass II
Reason for RecallDuring 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 Quantity71
Recall NumberF-0261-2013
Product Description#231 Bulk Cantalope 231 3 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 231
ClassificationClass II
Reason for RecallDuring 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 Quantity85
Recall NumberF-0262-2013
Product Description#075 Fruit Cup: Mixed Fruit 15.8 ounces #066 Fruit Cup: Mixed Fruit 9 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90466 and 0-11213-90457.
ClassificationClass II
Reason for RecallDuring 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 Quantity2559
Recall NumberF-0263-2013
Product Description#073 Fruit Cup: Cantalope Honeydew 15.8 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90462
ClassificationClass II
Reason for RecallDuring 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 Quantity560
Recall NumberF-0264-2013
Product Description#070 Fruit Cup: Honeydew 15.8 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90460
ClassificationClass II
Reason for RecallDuring 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 Quantity383
Recall NumberF-0265-2013
Product Description#068 Fruit Cup: Cantalope 15.8 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90459
ClassificationClass II
Reason for RecallDuring 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 Quantity807
Recall NumberF-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 InfoAll with sell by dates on or before 15-Sepwith UPC 0-11213-90455, 0-11213-90399, and 0-11213-90456.
ClassificationClass II
Reason for RecallDuring 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 Quantity4702 total
Recall NumberF-0267-2013
Product Description#064 Fruit Cup: Cantaloupe Honeydew Water Straw 9 ounces
Code InfoAll products with the sell by dates on or before 15-Sept with UPC 0-11213-90465
ClassificationClass II
Reason for RecallDuring 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 Quantity1269
Recall NumberF-0268-2013
Product Description#063 Fruit Cup: Cantaloupe Honeydew Watermelon 9 ounces
Code InfoAll products with the sell by dates on or before 15-Sept with UPC 0-11213-90464
ClassificationClass II
Reason for RecallDuring 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 Quantity1089
Recall NumberF-0269-2013
Product Description#061 Fruit Cup:Cantalope,Honeydew,Grape,Strawberry 9 ounces
Code InfoAll products with the sell by dates on or before 15-Sept with UPC 0-11213-90463
ClassificationClass II
Reason for RecallDuring 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 Quantity1305
Recall NumberF-0270-2013
Product Description#060 Fruit Cup Watermelon 9 ounces #072 Fruit Cup: Watermelon 15.8 ounces
Code InfoAll products with the sell by dates on or before 15-Sept with UPC 0-11213-90458 and 0-11213-90461.
ClassificationClass II
Reason for RecallDuring 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 Quantity1746
Recall NumberF-0271-2013
Product Description#055 10" Party Tray with No Dip 30 ounces
Code InfoAll products with the sell by dates on or before 15-Sept. with UPC 0-11213-90409
ClassificationClass II
Reason for RecallDuring 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 Quantity651
Recall NumberF-0272-2013
Product Description#048 Mixed Fruit Tray 20 ounces and #049 Mixed Fruit Tray 42 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90393 and 0-11213-90394
ClassificationClass II
Reason for RecallDuring 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 Quantity2059 (20 oz tray) and 1461 (42oz tray)
Recall NumberF-0273-2013
Product Description#033 Sugar Snap Peas 7 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90419
ClassificationClass II
Reason for RecallDuring 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 Quantity261
Recall NumberF-0274-2013
Product Description#029 Snow Peas 7 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90417
ClassificationClass II
Reason for RecallDuring 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 Quantity235
Recall NumberF-0275-2013
Product Description#027 Diced White Onions 6 ounces and #026 Diced Red Onions 6 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90415 and 0-11213-90414
ClassificationClass II
Reason for RecallDuring 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 Quantity492 (white onions) and 502 (red onions)
Recall NumberF-0276-2013
Product Description#025 Diced Colored Peppers 9 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90413
ClassificationClass II
Reason for RecallDuring 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 Quantity485
Recall NumberF-0277-2013
Product Description#024 Diced Pepper & Onions 9 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90412
ClassificationClass II
Reason for RecallDuring 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 Quantity494
Recall NumberF-0278-2013
Product Description#023 Soup Starter 8 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90411
ClassificationClass II
Reason for RecallDuring 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 Quantity164
Recall NumberF-0279-2013
Product Description#022 Salad Topper 8 ounces
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90410
ClassificationClass II
Reason for RecallDuring 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 Quantity443
Recall NumberF-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 InfoAll with sell by dates on or before 16-Sep with UPC 0-11213-08488, 0-11213-90381, 0-11213-08487, and 0-11213-08489.
ClassificationClass II
Reason for RecallDuring 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 Quantity3447
Recall NumberF-0281-2013
Product Description#017 Vegetable Tray with No Dip 2 pounds
Code InfoAll with sell by dates on or before 16-Sep with UPC 0-11213-90408
ClassificationClass II
Reason for RecallDuring 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 Quantity371
Recall NumberF-0282-2013
Product Description#011 Zucchini Stir,Fry 0.75 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90380
ClassificationClass II
Reason for RecallDuring 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 Quantity520
Recall NumberF-0283-2013
Product Description#010 Broccoli Stir Fry 0.75 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90378
ClassificationClass II
Reason for RecallDuring 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 Quantity534
Recall NumberF-0284-2013
Product Description#009 Colored Peppers 0.76 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90377
ClassificationClass II
Reason for RecallDuring 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 Quantity595
Recall NumberF-0285-2013
Product Description#008 Red-Yellow-Green Peppers, Onions 0.75 pounds
Code InfoAll with sell by dates on or before 15-Sep with UPC 0-11213-90379
ClassificationClass II
Reason for RecallDuring 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 Quantity676
Recall NumberF-0286-2013
Product Description#002 Broccoli, Cauliflower 0.75 pounds
Code InfoAll with sell by dates on or before 16-Sep with UPC 0-11213-08490
ClassificationClass II
Reason for RecallDuring 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 Quantity898
Recall NumberF-0287-2013
Product Description#747 Egg Salad Sandwich on White
Code InfoSell by 9/13/12
ClassificationClass II
Reason for RecallDuring 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 NumberF-0288-2013
Product Description#052 and #053, Party Tray with Fruit and Dip, 30 and 50 oz.
Code InfoSell by 9/15/12
ClassificationClass II
Reason for RecallDuring 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 NumberF-0289-2013

Class II Devices Event

Event ID63191
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date06-Jul-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmBeckman Coulter Inc.
CityBrea
StateCA
CountryUS
Distribution PatternWorldwide Distribution and US (nationwide) and the countries of China, France, Italy and Taiwan.
 

Associated Products

Product DescriptionUnicel 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 InfoSerial Numbers: 547-574 (UCTA)
ClassificationClass II
Reason for RecallThe 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 Quantity18 units
Recall NumberZ-0059-2013

Class II Food Event

Event ID63192
StatusTerminated
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date29-Jun-12
Initial Firm Notification of Consignee or Public Email
Recalling FirmLovin Oven, LLC
CityAzusa
StateCA
CountryUS
Distribution PatternNationwide in the US
 

Associated Products

Product DescriptionEarth's Best Organic Wheat Teething Biscuits, 6 pack, UPC # 23923-90015, HCG#C90615
Code InfoLot Codes: 29JUL12, 14AUG12
ClassificationClass II
Reason for RecallEarth's Best is recalling Earth's Best Organic Wheat Teething Biscuits because it may contain very small metal fragments.
Product Quantity8,904 units
Recall NumberF-0109-2013

Class II Food Event

Event ID63203
StatusCompleted
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date07-Jun-12
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmSUNFRESH NATURAL LLC.
CityPassaic
StateNJ
CountryUS
Distribution PatternNationwide
 

Associated Products

Product DescriptionSunFresh Natural Pitted Prunes Net wt. 6 oz. Distributed by: Sunfresh Natural LLC, Passaic, NJ 07055 Please visit us at: www.sunfreshnatural.com
Code InfoNo codes
ClassificationClass II
Reason for RecallPrunes 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 Quantity1200 bags
Recall NumberF-0297-2013

Class II Food Event

Event ID63206
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date06-Sep-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmLehi Valley Trading Co.
CityMesa
StateAZ
CountryUS
Distribution PatternUS States: AZ, NJ, NM, NJ, TX, LA, CA, WI, WA, VT, GA, and FL. No international distribution.
 

Associated Products

Product DescriptionLicorice 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 Info1) 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;
ClassificationClass II
Reason for RecallWe 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 QuantityAmounts distributed are listed in code information.
Recall NumberF-0120-2013

Class II Food Event

Event ID63218
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date18-Sep-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmRalcorp Frozen Bakery Products
CityDowners Grove
StateIL
CountryUS
Distribution PatternKentucky, Michigan, Ohio
 

Associated Products

Product DescriptionGFS 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 Infoon case: Reorder No. 577006, Baked 07/30/12, use by 07/30/2013; on muffin wrapper: 07/30/12
ClassificationClass II
Reason for RecallSome of the cases labeled as blueberry muffins actually contain banana nut muffins, resulting in undeclared tree nuts
Product Quantity1,542 cases
Recall NumberF-0119-2013

Class II Devices Event

Event ID63223
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date09-May-12
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmAesculap, Inc.
CityCenter Valley
StatePA
CountryUS
Distribution PatternWithin the US, product was distributed to PA and TN.
 

Associated Products

Product DescriptionColumbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
Code InfoNQ083R
ClassificationClass II
Reason for RecallThe 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 Quantity2
Recall NumberZ-0082-2013

Class II Devices Event

Event ID63225
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date02-Oct-09
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmTerumo Cardiovascular Systems Corporation
CityAnn Arbor
StateMI
CountryUS
Distribution PatternWorldwide distribution: USA (nationwide) including states of: CA, MI, NC, NJ, PA, and WI;and country of: EUROPE.
 

Associated Products

Product DescriptionTerumo 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 InfoNo lot/serial number; Catalog number: PN 816280
ClassificationClass II
Reason for RecallBackplate 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 Quantity33 units
Recall NumberZ-0071-2013

Class II Food Event

Event ID63245
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date20-Sep-12
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling FirmOregon Ice Cream, LLC
CityEugene
StateOR
CountryUS
Distribution PatternProduct was distributed to distribution centers in CA, CO, CT, IA, IN, NH, and PA.
 

Associated Products

Product DescriptionAlden'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:"***ORGANIC***Alden's ICE CREAM***COOKIES 'n CREAM***1.5 QTS (1.42L)***". The CUP of the recalled product is labeled in parts: "***ORGANIC***Alden's ICE CREAM***CHOLOCATE CHOCOLATE CHIP***MFD. BY OREGON ICE CREAM***EUGENE, OR 97402***1-800-282-2202***www.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 Info12243 printed at the bottom of the cup
ClassificationClass II
Reason for RecallAlden'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 Quantity1400 cases/3 cups
Recall NumberF-0298-2013

Class II Food Event

Event ID63250
StatusTerminated
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date05-Feb-12
Initial Firm Notification of Consignee or Public Visit
Recalling FirmBottling LLC dba Pepsi Beverages Company
CityPhoenix
StateAZ
CountryUS
Distribution PatternArizona
 

Associated Products

Product DescriptionDiet Crush Orange Soda, 12 oz cans
Code InfoAPR1612ttttPW011012 (tttt represents military time)
ClassificationClass II
Reason for RecallDr 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 Quantity1791 cases
Recall NumberF-0121-2013

Class II Devices Event

Event ID63255
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date19-Sep-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmTrumpf Medical Systems, Inc.
CityCharleston
StateSC
CountryUS
Distribution PatternNationwide 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 DescriptionHelion 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 InfoOndal 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).
ClassificationClass II
Reason for RecallIncidents regarding fractures of the front joint of the spring arm have been reported.
Product Quantity275 units
Recall NumberZ-0077-2013

Class II Food Event

Event ID63315
StatusOngoing
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date24-Sep-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmRichmond Baking of Georgia Inc
CityAlma
StateGA
CountryUS
Distribution PatternAZ, CA, FL, HI, ID, IL, IN, KS, MI, NJ, OR, PA, TN, TX, VA and WA.
 

Associated Products

Product DescriptionMJM 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 InfoLot code; 030813, Pouches coded: 13067GA12, 13067GA22, 13067GA32, 13067GA42, 13052 and 13067GA62.
ClassificationClass II
Reason for RecallProduct contains undeclared allergen: Soy Lecithin.
Product Quantity896 cases (150/1oz. packages per case)
Recall NumberF-0112-2013

Class II Devices Event

Event ID63359
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date26-Sep-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmMOOG Medical Devices Group
CitySalt Lake City
StateUT
CountryUS
Distribution PatternNationwide 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 InfoProduct Code/Lot Number: 340-4166/CF1022906; 340-4128-V/CRF10082001; 340-4165/CF1022905.
ClassificationClass II
Reason for RecallThis 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 Quantity12,000 sets
Recall NumberZ-0072-2013

Class II Devices Event

Event ID63365
StatusOngoing
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date25-Sep-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmTeleflex Medical
CityResearch Triangle Park
StateNC
CountryUS
Distribution PatternNationwide Distribution including the state of Nevada.
 

Associated Products

Product DescriptionHem-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 InfoCatalog No. 544240, Lot #01E1200585
ClassificationClass II
Reason for RecallProduct is being recalled due to the possibility that the tray may contain pinholes, compromising product sterility.
Product Quantity126 units
Recall NumberZ-0078-2013

Class II Drugs Event

Event ID63406
StatusOngoing
Product TypeDrugs
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date05-Oct-12
Initial Firm Notification of Consignee or Public E-Mail
Recalling FirmEarthborn Products, Inc.
CitySan Diego
StateCA
CountryUS
Distribution PatternNationwide
 

Associated Products

Product DescriptionColloidal 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 InfoLot #: 009-22-A011, 011-28-A011, 004-01-A012, 005-24-A012, 007-24-A012, and 008-08-A012.
ClassificationClass II
Reason for RecallMarketed 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 Quantity161 gallons
Recall NumberD-009-2013

Class III Biologics Event

Event ID40195
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date04-May-05
Initial Firm Notification of Consignee or Public FAX
Recalling FirmCommunity Blood Bank of Lancaster County Medical Society
CityLincoln
StateNE
CountryUS
Distribution PatternNE
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code Info3697502
ClassificationClass III
Reason for RecallBlood product, viral testing performed, interpreted, or documented incorrectly, were distributed.
Product Quantity1 unit
Recall NumberB-2410-12
Product DescriptionPlatelets Pheresis Leukocytes Reduced Irradiated
Code Info3697525; 3697482; 3697482
ClassificationClass III
Reason for RecallBlood product, viral testing performed, interpreted, or documented incorrectly, were distributed.
Product Quantity3 units
Recall NumberB-2411-12
Product DescriptionPlatelets Pheresis Leukocytes Reduced
Code Info3697528(Part A); 3697528(Part B)
ClassificationClass III
Reason for RecallBlood product, viral testing performed, interpreted, or documented incorrectly, were distributed.
Product Quantity2 units
Recall NumberB-2412-12

Class III Biologics Event

Event ID41806
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date27-Mar-06
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmUniversity of Colorado Hospital
CityAurora
StateCO
CountryUS
Distribution PatternCO
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced, irradiated
Code Info09FF59915;09GJ67158
ClassificationClass III
Reason for RecallBlood products, which were labeled with incorrect or missing information were distributed.
Product Quantity2 units
Recall NumberB-2431-12

Class III Biologics Event

Event ID44021
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date11-Jan-07
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmMississippi Valley Regional Blood Center
CityDavenport
StateIA
CountryUS
Distribution PatternPennsylvania
 

Associated Products

Product DescriptionPlatelets
Code InfoLM44607
ClassificationClass III
Reason for RecallBlood product, which was manufactured from whole blood units in which collection extended beyond the allowable time limits, was distributed.
Product Quantity1 Unit
Recall NumberB-2430-12

Class III Biologics Event

Event ID47618
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date19-Feb-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternKansas
 

Associated Products

Product DescriptionFresh Frozen Plasma
Code InfoW045007056807;W045007056809
ClassificationClass III
Reason for RecallBlood products, for which storage condition was outside the acceptable range, were distributed.
Product Quantity2 Units
Recall NumberB-2507-12

Class III Biologics Event

Event ID48854
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date13-May-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Bank of Lancaster County Medical Society
CityLincoln
StateNE
CountryUS
Distribution PatternNE
 

Associated Products

Product DescriptionPlatelets Pheresis Leukocytes Reduced Irradiated
Code InfoW087908300822
ClassificationClass III
Reason for RecallBlood product, labels applied to blood unit or product with incorrect or missing information, was distributed.
Product Quantity1 unit
Recall NumberB-2409-12

Class III Biologics Event

Event ID49809
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date25-Aug-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternMO
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW045008045744
ClassificationClass III
Reason for RecallBlood product, manufactured without additive solution, was distributed.
Product Quantity1 Unit
Recall NumberB-2449-12

Class III Biologics Event

Event ID50642
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date07-Oct-08
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center Of Gtr KC
CityKansas City
StateMO
CountryUS
Distribution PatternMissouri
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW045008091475
ClassificationClass III
Reason for RecallBlood product, manufactured without additive solution, was distributed.
Product Quantity1 Unit
Recall NumberB-2450-12

Class III Devices Event

Event ID62516
StatusCompleted
Product TypeDevices
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date15-Nov-11
Initial Firm Notification of Consignee or Public Letter
Recalling FirmSunquest Information Systems, Inc.
CityTucson
StateAZ
CountryUS
Distribution PatternNationwide distribution
 

Associated Products

Product DescriptionSunquest Laboratory : intended for use by professionals working in a clinical laboratory.
Code InfoVersions 6.4.0 and later
ClassificationClass III
Reason for RecallOnline 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 Quantity127 sites
Recall NumberZ-0073-2013

Class III Biologics Event

Event ID62635
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date21-Jun-12
Initial Firm Notification of Consignee or Public Telephone
Recalling FirmCommunity Blood Center
CityDayton
StateOH
CountryUS
Distribution PatternOhio
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced Irradiated
Code InfoW035412042113;
ClassificationClass III
Reason for RecallBlood product, labeled with an extended expiration date following irradiation, was distributed.
Product Quantity1
Recall NumberB-2383-12

Class III Drugs Event

Event ID63224
StatusOngoing
Product TypeDrugs
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date20-Sep-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmSandoz Incorporated
CityBroomfield
StateCO
CountryUS
Distribution PatternNationwide
 

Associated Products

Product DescriptionChildren'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 InfoNDC 0781-5283-64 lots: BT2862, BT7986, BT7994, BW0652, CC1961, and CA3437; NDC 0904-5878-33 lot BW0665.
ClassificationClass III
Reason for RecallImpurity/Degradation; exceeded impurity specification at the 8 and 15 month time points (betacyclodextrin ester 1&2)
Product Quantity67,937 x 30 tablet cartons; 24,640 x 5 tablet cartons
Recall NumberD-008-2013

Class III Food Event

Event ID63227
StatusTerminated
Product TypeFood
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date29-Mar-12
Initial Firm Notification of Consignee or Public Letter
Recalling FirmSouthwind Foods LLC dba Great American Seafood Imports Co.
CityVernon
StateCA
CountryUS
Distribution PatternCA, AZ, TX
 

Associated Products

Product DescriptionFrozen Red Cod Fillet (Red Snapper) Individually Quick Frozen was labeled and identified as Snapper FILL IQF (ROCKFISH). 1/10 lb, code #14343.
Code InfoLot#90595
ClassificationClass III
Reason for RecallSouthwind Foods is recalling Frozen Snapper Fill IQF (Rock Fish) because it mislabeled and misleading.
Product Quantity145 cases
Recall NumberF-0123-2013

Mixed Classification Biologics Event

Event ID62740
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date24-Jul-12
Initial Firm Notification of Consignee or Public FAX
Recalling FirmBlood Assurance Inc
CityChattanooga
StateTN
CountryUS
Distribution PatternFlorida; Indiana
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW043211068074;
ClassificationClass II
Reason for RecallBlood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity1
Recall NumberB-2478-12
Product DescriptionRecovered Plasma
Code InfoW043211068074;
ClassificationClass III
Reason for RecallBlood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity1
Recall NumberB-2479-12

Mixed Classification Biologics Event

Event ID62741
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date13-Jul-11
Initial Firm Notification of Consignee or Public FAX
Recalling FirmBlood Assurance Inc
CityChattanooga
StateTN
CountryUS
Distribution PatternTennessee; Indiana
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW043210092064;
ClassificationClass II
Reason for RecallBlood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity1
Recall NumberB-2480-12
Product DescriptionRecovered Plasma
Code InfoW043210092064;
ClassificationClass III
Reason for RecallBlood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Product Quantity1
Recall NumberB-2481-12

Mixed Classification Biologics Event

Event ID62743
StatusTerminated
Product TypeBiologics
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date20-Jun-12
Initial Firm Notification of Consignee or Public FAX
Recalling FirmBlood Assurance Inc
CityChattanooga
StateTN
CountryUS
Distribution PatternSouth Carolina; New York; Indiana
 

Associated Products

Product DescriptionRed Blood Cells Leukocytes Reduced
Code InfoW043211038237; W043210095642;
ClassificationClass II
Reason for RecallBlood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed
Product Quantity2
Recall NumberB-2483-12
Product DescriptionRecovered Plasma
Code InfoW043211038237; W043210095642;
ClassificationClass III
Reason for Recall
Product Quantity2
Recall NumberB-2484-12
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