Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K101438 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Femoral Nail, RIGHT T2 GTN 8x300 mm. Catalog Number: 1851-0830S. | 2 | 06/10/2025 | Stryker GmbH |
| Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S. | 2 | 06/10/2025 | Stryker GmbH |
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