Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K982468 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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IMMULITE 2000 Thyroglobulin (US)- For in vitro diagnostic use with the IMMULITE 2000 Systems Analyz... | 2 | 01/11/2023 | Siemens Healthcare Diagnostics, Inc. |
IMMULITE 2000 Thyroglobulin (OUS). For in vitro diagnostic use with the IMMULITE 2000 Systems Analyz... | 2 | 01/11/2023 | Siemens Healthcare Diagnostics, Inc. |
IMMULITE ® 2000/IMMULITE ® 2000 XPi TG | 2 | 05/04/2018 | Siemens Healthcare Diagnostics, Inc. |
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