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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 24 Results
Related Medical Device Recalls
 
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Product Description
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FDA Recall
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Z-1685-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi TG 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1681-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi Gastrin 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1676-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi Folic Acid 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1679-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi CEA 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1691-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi BR-MA (CA15-3) 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1675-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi Anti HBc 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1674-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi 3g Allergy specific IgE Universal Kit 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1686-2018 - IMMULITE ® /IMMULITE ® 1000 Vitamin B12 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1684-2018 - IMMULITE ® /IMMULITE ® 1000 TG 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1682-2018 - IMMULITE ® /IMMULITE ® 1000 OM-MA (CA125) 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
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