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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 24 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1678-2018 - IMMULITE ¿ /IMMULITE ¿ 1000 CEA 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1679-2018 - IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi CEA 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1680-2018 - IMMULITE ¿ /IMMULITE 1000 ¿ Gastrin 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1681-2018 - IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Gastrin 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1682-2018 - IMMULITE ¿ /IMMULITE ¿ 1000 OM-MA (CA125) 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1683-2018 - IMMULITE 2000/IMMULITE ¿ 2000 XPi OM-MA (CA125) 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1684-2018 - IMMULITE ¿ /IMMULITE ¿ 1000 TG 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1685-2018 - IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi TG 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1686-2018 - IMMULITE ¿ /IMMULITE ¿ 1000 Vitamin B12 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1687-2018 - ADVIA Centaur¿ Cyclosporine 2 05/04/2018 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
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