Zimmer/CAS Power Cord, Sesamoid Plasty, NA, Zimmer/CAS, Montreal (Quebec), Canada; REF 20-8000-070-12. The device is the
FDA device recall Z-0558-2010 · posted 2009-12-22 · Terminated
Recall details
- Recalling firm
- Zimmer Inc.
- Reason for recall
- The power cord female receptacle is not recessed sufficiently and may present a shock hazard.
- Action taken
- Zimmer sales staff were notified by letter dated 11/2/09 and instructed to locate the units and to upgrade the cords and to notify consignees by copy of a letter addressed to risk managers and dated 11/2/09.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- HAW
- Quantity affected
- 71
- Distribution
- Nationwide.
- Date initiated
- 2009-11-02
- Date posted
- 2009-12-22
- Date terminated
- 2010-10-15
- Location
- Warsaw, IN
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
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