Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K123347 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Drill, 3.2x145mm, AO, Item Number 502015650 | 2 | 05/23/2019 | Zimmer GmbH |
| Drill, 2.7x125mm, AO, Item Number 502015217 | 2 | 05/23/2019 | Zimmer GmbH |
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