Zimmer Inc. Zimmer NEXGEN Complete Knee Solution articular surface insertion instrument, non-sterile. This device is a surgical instrument used during knee arthroplasty procedures to snap or lock the polyethylene bearing surface into the retaining rail on a metal tibial plate. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Zimmer NEXGEN Complete Knee Solution articular surface insertion instrument, non-sterile. This device is a surgical instrument used during knee arthroplasty procedures to snap or lock the polyethylene bearing surface into the retaining rail on a metal tibial plate.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
Lots 60577285, 60582624, 60587308, 60603255 and 60610860.
Products Sold
Lots 60577285, 60582624, 60587308, 60603255 and 60610860.
Zimmer Inc. is recalling Zimmer NEXGEN Complete Knee Solution articular surface insertion instrument, non-sterile. This devi due to The instrument is prone to fracture during use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The instrument is prone to fracture during use.
Recommended Action
Per FDA guidance
Direct and hospital consignees were notified via email or letter on 5/16/08 to cease use and return the instruments. Contact Kevin W. Escapule at 800-846-4637 if you have questions.
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 noticePage updated: Jan 10, 2026