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FDA device recall Z-0649-2007 · posted 2007-03-28 · Terminated
Recall details
- Recalling firm
- Zimmer Inc.
- Reason for recall
- The device was cut to an incorrect angle, which may result in an incorrect bone cut.
- Action taken
- Product was removed from customer location during visit on 10/10/2006.
- Root cause
- Other
- Status
- Terminated
- Product code
- JWH
- Quantity affected
- 1
- Distribution
- One medical facility in Michigan.
- Date initiated
- 2006-10-10
- Date posted
- 2007-03-28
- Date terminated
- 2007-12-04
- Location
- Warsaw, IN
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