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U.S. Department of Health and Human Services

Class 2 Device Recall Video Cart MultiSpecialty

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  Class 2 Device Recall Video Cart MultiSpecialty see related information
Date Initiated by Firm February 23, 2010
Date Posted January 04, 2011
Recall Status1 Terminated 3 on March 22, 2012
Recall Number Z-0849-2011
Recall Event ID 56829
Product Classification Camera, surgical and accessories - Product Code KQM
Product Video Cart Multi-Specialty product labeling is as follows:
REF, VP6502, QTY1, Video Cart Multi-Specialty, 120V, Rx ONLY,
These Video Carts are intended for storage of Endoscopic equipment that is used in single or multiple surgical specialties

MANUFACTURED FOR: Linvatec, LINVATEC CORPORATION, LARGO, FL 33773 USA.
Code Information Video Cart Multi-Specialty (Catalog Number : VP6502)  Serial #: 04090102 04090202 04090302 04090402 04090502 04090602 04090702 04090802 04090902 04091002 04091102 04091202 04091302 04091402 04091502 04091602 04091702 04110102 04110202 04110302 04110402 04110502 04110602 04110702 04110802 04110902 04111002 04111102 04111202 04111302 04111402 04111502 04111602 04111702 04111802 04111902 05030102 05030202 05030302 05030402 05030502 05030602 05030702 05030802 05030902 05031002 05031102 05031202 05031302 05031402 05031502 05031602 05031702 05031802 05031902 05050102 05050202 05050302 05050402 05050502 05050602 05050802 05050902 05051002 05060102 05060202 05060302 05070102 05070202 05070402 05070502 05070602 05080102 05080202 05080302 05080402 05080502 05080602 05080702 05090102 05090202 05090302 05090402 05090502 05090602 05090702 06020102 06020202 06020302 06020402 06020502 06020602 06020802 06020902 06021002 06040102 06040202 06040302 06040402 06040502 06050102 06050202 06050302 06050402 06050502 06050602 06050702 06050802 06050902 06070102 06070202 06070302 06070402 06070502 06070602 06080102 06080202 06080302 06080402 06080502 06080602 06080702 06080802 06080902 06081002 06090102 06090202 06090302 06090402 06090502 06090602 06090702 06090802 06090902 06091002 06091102 06091202 06100102 06100202 06100302 06100502 06100702 06100802 06100902 06101002 06101102 06110102 06110202 06110302 06110402 06110502 06110602 06110702 06110802 06110902 06111002 06111102 06111202 06111302 06111402 06111502 06111602 06111702 06111802 06120102 06120202 06120302 06120402 07120102 08010102 08010202 08010302 08010402 
Recalling Firm/
Manufacturer		 Linvatec Corp. dba ConMed Linvatec
11311 Concept Blvd
Largo FL 33773-4908
For Additional Information Contact Roger Murphy
727-399-5205
Manufacturer Reason
for Recall		 ConMed Linvatec, Endoscopy Division, dba. ConMed Linvatec, Largo, Florida is recalling five products: (1.) Video Cart Premium 120 VAC (VP6501), (2.) Video Cart Multi-Specialty 120 VAC (VP6502), (3.) Video Cart Articulating Arm 120V (VP6504), (4.) Video Cart (VP8500), and (5.) Power Cord Assembly Self Retracting (VP6547). These products are being recalled due to there is a possibility that the Vid
FDA Determined
Cause 2		 Component design/selection
Action ConMed Linvatec sent URGENT MEDICAL DEVICE CORRECTION NOTIFICATION letters to their customers by FedEx. The letter identified the product, the problem, and the action to be taken by the customer. Customers were asked to review their plugs for damage and determine if they were affected. Distributors were asked to contact affected customers and schedule delivery of their replacement plugs within 30 days. If the account no longer has the product in their possession, or if they have transferred the product, they were asked to respond as such via a Reply form. Customers were asked to document delivery of replacement plugs on the Sales Rep Reply Form and mail back or return by fax to 1-888-370-3062. For questions regarding this recall call the Customer Service Department at 1-888-292-0100 or e-mail Custserv1@Invatec.com.
Quantity in Commerce 173 carts
Distribution Worldwide Distribution - USA including AK, AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV, AND WY and the countries of Canada, Chile, Colombia, Denmark, Korea, Mexico, Singapore, South Africa, United Arab Emirates, and Venezuela.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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