T2 Tibia Nail, Standard 9 x 300 mm, T2 Tibia System, Catalog No. 1822-0930S.
This recall has been terminated (originally issued October 15, 2003).
- Company
- Stryker Howmedica Osteonics
- Recall Initiated
- August 4, 2003
- Posted
- October 15, 2003
- Terminated
- September 30, 2003
- Recall Number
- Z-1295-03
- Quantity
- 6
- Firm Location
- Mahwah, NJ
- Official Source
- View on FDA website ↗
Reason for Recall
The device does not have an oblong hole for dynamic locking as required.
Distribution
The 6 units were distributed to Howmedica Branch and sales agents located in PA, VA, GA, KS, and CA.
Lot / Code Info
Lot K884459
Root Cause
Other
Action Taken
Product recall letters and Product accountability forms were sent via FedEx on 8/4/2003 with return receipt.
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