Femoral Resection Guide, Scorpio L.R.S. Instrumentation.
This recall has been terminated (originally issued August 21, 2003).
- Company
- Stryker Howmedica Osteonics
- Recall Initiated
- July 17, 2003
- Posted
- August 21, 2003
- Terminated
- September 3, 2003
- Recall Number
- Z-1143-03
- Quantity
- 102
- Firm Location
- Mahwah, NJ
- Official Source
- View on FDA website ↗
Reason for Recall
Scorpio Femoral Resection Guides have the potential to remove more bone than necessary.
Distribution
The catalog numbers were sent to Howmedica Osteonics Sales Representatives/agents, one Canada Howmedica Sales Representative, and one International Howmedica location in Ireland.
Lot / Code Info
Catalog No: 8050-5103; 8050-5105; 8050-5107; 8050-5109; 8050-5111; 8050-5113.
Root Cause
Other
Action Taken
Product recall letters and product accountability forms were sent via FedEx to all Branches/sales agents on July 17, 2003. For the Canadian and International customers, the recall notification was also sent on July 17, 2003. All devices are to be returned to Howmedica Osteonics, Mahwah, NJ.
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