Zimmer Inc. NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272518. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272518.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
Lot 97000414.
Products Sold
Lot 97000414.
Zimmer Inc. is recalling NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, i due to The device was cut to an incorrect angle, which may result in an incorrect bone cut.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The device was cut to an incorrect angle, which may result in an incorrect bone cut.
Recommended Action
Per FDA guidance
Product was removed from customer location during visit on 10/10/2006.
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
IN, MI
Page updated: Jan 10, 2026