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Terminated

NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272522.

FDA Recall Z-0651-2007 · Posted 2007-03-28

Recalling FirmZimmer Inc.
Recall StatusTerminated
Product CodeJWH
Date Initiated2006-10-10
Date Terminated2007-12-04
Product Quantity1

Reason for Recall

The device was cut to an incorrect angle, which may result in an incorrect bone cut.

Firm Action

Product was removed from customer location during visit on 10/10/2006.

Root Cause

Other

Distribution Pattern

One medical facility in Michigan.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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