Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K913459 |
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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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ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic, a quantitative technique for determining th... | 2 | 12/19/2017 | BioMerieux SA |
ETEST OXACILLIN OX 256 US F100 In vitro diagnostic, a quantitative technique for determining ... | 2 | 12/19/2017 | BioMerieux SA |
ETEST Gentamicin GM256 FOAM packaging, Product Name: ETEST Gentamicin GM 0.016-256(low). ETEST is a... | 2 | 03/21/2017 | BioMerieux SA |
ETEST Cephalotin CE 256 Foam packaging, Product Name: ETEST Cephalothin CE 0.016-256. ETEST is a qu... | 2 | 03/21/2017 | BioMerieux SA |
ETEST CLINICAL ERYTHROMYCIN EM 256 US S30, CATALOG 412333 | 2 | 01/04/2023 | Biomerieux Inc |
ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412252 | 2 | 01/04/2023 | Biomerieux Inc |
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