Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K122698 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Aequalis Ascend Flex Shoulder System Reversed Platform (Reversed Tray component) Rx Only Sterile M... | 2 | 07/12/2021 |
FEI # 3000718467 Tornier, Inc |
| Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475 DWF601B 3700386944482 D... | 2 | 11/14/2019 |
FEI # 3000718467 Tornier, Inc |
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