Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K161742 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ... | 2 | 10/13/2023 | Tornier, Inc |
| Ratcheting Screwdriver Handle, provided in the Aequalis Perform Reversed kit | 2 | 06/01/2022 | Tornier, Inc |
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