Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K222427 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.25M... | 2 | 01/12/2024 |
FEI # 3008021110 Limacorporate S.p.A |
| REF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate, STERILE R | 2 | 06/27/2023 |
FEI # 3008021110 Limacorporate S.p.A |
| REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R | 2 | 06/27/2023 |
FEI # 3008021110 Limacorporate S.p.A |
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