Recall Z-0901-03 ยท HWA Impactor
Stryker Howmedica Osteonics
Trident Insert Impactor
| Date | May 29, 2003 (initiated Apr 28, 2003) |
| Status | Terminated |
| Reason | The ball retaining sleeve on the Trident Insert Impactor can possibly disassemble. |
| Root cause | Other |
| Action | Howmedica sent recall letters and acknowledgement forms via FedEx on April 29, 2003 with return receipt. |
| Quantity | 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, Japan, New Zealand, Switzerland, Portugal, England, Chile, and Brazil. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.