Medical Device Recalls
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1 result found
510(K) Number: K151907 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202 | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
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