Medical Device Recalls
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1 result found
510(K) Number: K111711 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| JOURNEY II BCS ARTICULAR INSERT, LEFT 10 MM SIZE 5-6, REF 74027262; knee prosthesis | 2 | 10/24/2023 |
FEI # 1020279 Smith & Nephew, Inc. |
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