FDA Recall
Terminated
Zimmer/CAS Power Cord, Sesamoid Plasty, NA, Zimmer/CAS, Montreal (Quebec), Canada; REF 20-8000-070-12. The device is the power cord component for the Sesamoid Plasty CAS workstation which connects the workstation to the power mains.
Recall: Z-0558-2010
·
Initiated November 2, 2009
Recall
- Recall Number
- Z-0558-2010
- Event Number
- 53687
- Firm
- Zimmer Inc.
- FEI Number
- 1000220733
- Product Code
- HAW
- Status
- Terminated
- Root Cause
- Device Design
- Initiated
- November 2, 2009
- Posted
- December 22, 2009
- Terminated
- October 15, 2010
- Address
- 345 E Main St, Warsaw, IN, 46580-2746
Description
Zimmer/CAS Power Cord, Sesamoid Plasty, NA, Zimmer/CAS, Montreal (Quebec), Canada; REF 20-8000-070-12. The device is the power cord component for the Sesamoid Plasty CAS workstation which connects the workstation to the power mains.
Reason
The power cord female receptacle is not recessed sufficiently and may present a shock hazard.
Action
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.
Distribution
Nationwide.
Quantity
71