Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K122398 |
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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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RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 100 -Intended for in vitro diagnostic u... | 2 | 12/21/2023 | Siemens Healthcare Diagnostics Inc |
RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 750-Intended for in vitro diagnostic use... | 2 | 12/21/2023 | Siemens Healthcare Diagnostics Inc |
RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for in vitro diagnostic use... | 2 | 12/21/2023 | Siemens Healthcare Diagnostics Inc |
RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for in vitro diagnostic use... | 2 | 12/21/2023 | Siemens Healthcare Diagnostics Inc |
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