Howmedica Osteonics Corp. Recall: TRIDENTII PSL CLUSTER58F-Indicated for use in primary an
Howmedica Osteonics Corp. Recall: TRIDENTII PSL CLUSTER58F-Indicated for use in primary an is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Howmedica Osteonics Corp.; Product: TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Cat
| Recalling firm | Howmedica Osteonics Corp. |
|---|---|
| Product | TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F |
| Reason for recall | The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Nationwide Foreign: Netherlands, Canada, Singapore, Spain, Sweden, UK |
| Recall initiated | 20240227 |
| Recall number | Z-1631-2024 |
| Category | device |
| State | NJ |
| Country | United States |
$29/mo
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