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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 24 of 24 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-1679-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi CEA 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-1681-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi Gastrin 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
Z-1685-2018 - IMMULITE ® 2000/IMMULITE ® 2000 XPi TG 2 05/04/2018 Siemens Healthcare Diagnostics, Inc.
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