Trident Insert Impactor
FDA device recall Z-0901-03 · posted 2003-05-29 · Terminated
Recall details
- Recalling firm
- Stryker Howmedica Osteonics
- Reason for recall
- The ball retaining sleeve on the Trident Insert Impactor can possibly disassemble.
- Action taken
- Howmedica sent recall letters and acknowledgement forms via FedEx on April 29, 2003 with return receipt.
- Root cause
- Other
- Status
- Terminated
- Product code
- HWA
- Quantity affected
- 1758
- Distribution
- The product has been distributed the Howmedica branches and sales reps, hospitals, and International Howmedica distributors located in Sweden, China, France, Netherlands, Germany, Spain, Australia, Ja
- Date initiated
- 2003-04-28
- Date posted
- 2003-05-29
- Date terminated
- 2003-11-12
- Location
- Mahwah, NJ
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