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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 94 Results
Related Medical Device Recalls
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Product Description
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Z-0806-2023 - BIOBALL B.SPIZIZENII NCTC 10400 550X20, CATALOG 56012 2 01/04/2023 Biomerieux Inc
Z-0832-2023 - BIOBALL K.RHIZOPHILA (30X20), CATALOG 412690 2 01/04/2023 Biomerieux Inc
Z-0807-2023 - BIOBALL P.AERUGINOSA NCTC 12924 550X20, CATALOG 56017 2 01/04/2023 Biomerieux Inc
Z-0869-2023 - DCOUNT SYSTEMS REAGENTS CHEMCHROME V14 (6X1.8ML), CATALOG 306-R1026-01 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-0846-2023 - ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30, CATALOG 419046 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
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