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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 94 Results
Related Medical Device Recalls
 
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Z-0785-2023 - API 20 C AUX 25 STRIPS+25 MEDIA, CATALOG 20210 2 01/04/2023 Biomerieux Inc
Z-0784-2023 - API 20 E 25 STRIPS, CATALOG 20100 2 01/04/2023 Biomerieux Inc
Z-0810-2023 - API JAMES 2AMP, CATALOG 70542 2 01/04/2023 Biomerieux Inc
Z-0783-2023 - API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300 2 01/04/2023 Biomerieux Inc
Z-0809-2023 - API NIT1 NIT2 REAGENTS, CATALOG 70442 2 01/04/2023 Biomerieux Inc
Z-0786-2023 - API STAPH 25 STRIPS+25 MEDIA, CATALOG 20500 2 01/04/2023 Biomerieux Inc
Z-0808-2023 - API VP1 VP2 REAGENTS, CATALOG 70422 2 01/04/2023 Biomerieux Inc
Z-0812-2023 - ASTUTE REAGENT ASTUTE ELECTRONIC QUALITY CTRL DEVICE US, CATALOG 400016 2 01/04/2023 Biomerieux Inc
Z-0862-2023 - ASTUTE REAGENT NEPHROCHECK LIQUID CONTROLS KIT US, CATALOG 500013 2 01/04/2023 Biomerieux Inc
Z-0805-2023 - BIOBALL A.BRASILIENSIS NCPF 2275 550X20, CATALOG 56011 2 01/04/2023 Biomerieux Inc
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