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U.S. Department of Health and Human Services

Class 2 Device Recall ARTHROKNIFE

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 Class 2 Device Recall ARTHROKNIFEsee related information
Date Initiated by FirmJanuary 28, 2010
Date PostedAugust 24, 2010
Recall Status1 Terminated 3 on December 15, 2010
Recall NumberZ-2261-2010
Recall Event ID 54701
Product Classification Arthroscope - Product Code HRX
ProductREF 70-0077-103, 3mm ARTHRO-KNIFE SHEATHED KNIFE, SERRATED, STRAIGHT, 2-SIDED, STERILE, Rx ONLY. CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908 USA. Intended for use in orthaepedic surgery where a cutting instrument is required.
Code Information Lot Number: 55197,  55198,  55199,  70878,  70880,  70879,  89406,  89407,  89408,  89405,  94740,  94744,  94742,  94743,  107457,  106507,  106511,  106509,  106510,  106508,  118010,  118011,  118014,  118012,  124483, and  124481.  
Recalling Firm/
Manufacturer		 Linvatec Corp. dba ConMed Linvatec
11311 Concept Blvd
Largo FL 33773-4908
For Additional Information ContactRoger Murphy
727-392-6464
Manufacturer Reason
for Recall		This recall was due to the possibility that multiple products may have a breach in the poly-Tyvek pouch that could potentially compromise the sterility of the contents.
FDA Determined
Cause 2		Material/Component Contamination
ActionEach consignee will be notified of the recall by an Urgent Medical Device Recall Notification letter sent by FedEx or an equivalent method. The letter identified the affected product, explained the reason for recall, and health risk. Consignees were instructed to examine their inventory and segregate the affected product for return. Customers are to complete and return the Reply Form and to notify their customers if the product was further distributed. Consignees are instructed to return any remaining product to ConMed Linvatec. Questions should be directed to the Customer Service department at 800-535-8536.
Quantity in Commerce35,451 total
DistributionWorldwide Distribution -- United Arab Emirates, Austria, Australia, Belgium, Canada, Switzerland, Germany, Denmark, Spain, Finland, France, United Kingdom, Hong Kong, Ireland, Israel, India, Italy, Republic of Korea, Netherlands, Portugal, Serbia, Singapore, Slovenia, El Salvador, Thailand, Taiwan, South Africa, and throughout the U.S.
Total Product Life CycleTPLC 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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