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U.S. Department of Health and Human Services

Medical Device Recalls
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71 to 80 of 94 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Z-0822-2023 - ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331 2 01/04/2023 Biomerieux Inc
Z-0851-2023 - ETEST CLINICAL ERAVACYCLINE ERV US S30, CATALOG 421553 2 01/04/2023 Biomerieux Inc
Z-0863-2023 - ETEST CLINICAL COLISTIN CO 256 US B100, CATALOG 537348 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-0841-2023 - ETEST CLINICAL CEFTOLOZANE/TAZO C/T US S30, CATALOG 414445 2 01/04/2023 Biomerieux Inc
Z-0846-2023 - ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30, CATALOG 419046 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-0819-2023 - ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412252 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-0817-2023 - ETEST CLINICAL AMIKACIN AK 256 US S30, CATALOG 412218 2 01/04/2023 Biomerieux Inc
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