Medical Device Recalls
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1 result found
510(K) Number: K802665 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usag... | 2 | 04/16/2021 |
FEI # 1018233 C.R. Bard, Inc. |
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