Zimmer Inc. Zimmer NexGen Complete Knee Solution Legacy Knee - Posterior Stabilized LPS-Flex Femoral Component Precoat, Size D left , sterile, Zimmer, Warsaw, IN; REF 00-5960-014-51. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Zimmer NexGen Complete Knee Solution Legacy Knee - Posterior Stabilized LPS-Flex Femoral Component Precoat, Size D left , sterile, Zimmer, Warsaw, IN; REF 00-5960-014-51.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
Lot 61208295.
Products Sold
Lot 61208295.
Zimmer Inc. is recalling Zimmer NexGen Complete Knee Solution Legacy Knee - Posterior Stabilized LPS-Flex Femoral Component P due to The implant surface may not have been polished adequately, which could result in increased wear and polyethylene debris generation.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The implant surface may not have been polished adequately, which could result in increased wear and polyethylene debris generation.
Recommended Action
Per FDA guidance
Consignees were notified by phone beginning on 4/17/09 and email and letter notifications were sent on 4/22/09. A dear surgeon letter entitled Urgent: Medical Device Recall, dated April 28, 2009, is being sent to implanting surgeons recommending patient monitoring. Consignees are to return the response form indicating their receipt of the notification. Questions or concerns should be directed to (800) 846-4637 or www.zimmer.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, CA, CO, HI, IL, IN, MI, MN, MS, NJ, NM, NY, OH, OR, PA
Page updated: Jan 10, 2026