Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K121392 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. NOVATION GXL ... | 2 | 09/09/2022 |
FEI # 1038671 Exactech, Inc. |
| Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers... | 2 | 07/22/2021 |
FEI # 1038671 Exactech, Inc. |
| Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers... | 2 | 07/22/2021 |
FEI # 1038671 Exactech, Inc. |
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