Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K980348 |
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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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| ETEST Vancomycin VA 256 FOAM packaging, Product Name: ETEST Vancomycin VA 0.016-256. ETEST is a qua... | 2 | 03/21/2017 |
FEI # 1000611339 BioMerieux SA |
| ETEST CLINICAL VANCOMYCIN VA 256 US S30, CATALOG 412486 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
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