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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 94 Results
Related Medical Device Recalls
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Product Description
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Recall
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FDA Recall
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Z-0813-2023 - PPM INDUSTRY COMBOURG LPT BROTH (4X3L), CATALOG 410849 2 01/04/2023 Biomerieux Inc
Z-0814-2023 - VITEK MS CLINICAL REAGENT VITEK MS-DS, CATALOG 410893 2 01/04/2023 Biomerieux Inc
Z-0815-2023 - VITEK MS CLINICAL REAGENT VITEK MS-CHCA, CATALOG 411071 2 01/04/2023 Biomerieux Inc
Z-0816-2023 - VITEK MS CLINICAL REAGENT VITEK MS-FA, CATALOG 411072 2 01/04/2023 Biomerieux Inc
Z-0817-2023 - ETEST CLINICAL AMIKACIN AK 256 US S30, CATALOG 412218 2 01/04/2023 Biomerieux Inc
Z-0818-2023 - ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412240 2 01/04/2023 Biomerieux Inc
Z-0819-2023 - ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412252 2 01/04/2023 Biomerieux Inc
Z-0820-2023 - ETEST CLINICAL BENZYLPENICIL PG 256 US S30, CATALOG 412262 2 01/04/2023 Biomerieux Inc
Z-0821-2023 - ETEST CLINICAL CEFTRIAXONE TX 32 US S30, CATALOG 412302 2 01/04/2023 Biomerieux Inc
Z-0822-2023 - ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331 2 01/04/2023 Biomerieux Inc
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