Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K102668 |
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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 Tobramycin TM256 FOAM packaging, Product Name: ETEST Tobramycin TM 0.016-256(low). ETEST is a... | 2 | 03/21/2017 |
FEI # 1000611339 BioMerieux SA |
| ETEST CLINICAL TOBRAMYCIN TM 256 US S30, CATALOG 412478 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
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