Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K190298 |
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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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Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly | 2 | 07/14/2023 | Beckman Coulter Biomedical GmbH |
Beckman Coulter DxA Automation System, DxA 5000 Fit, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnl... | 2 | 07/14/2023 | Beckman Coulter Biomedical GmbH |
DxA 5000 (DxA Automation System, DxA 5000 fit), "For in Vitro Diagnostic Use", Reference Numbers: B8... | 2 | 09/30/2021 | Beckman Coulter Inc. |
DxA 5000; Catalog Number:B50516; UDI:15099590707118 - Product Usage: The DxA 5000 is a high-speed, m... | 2 | 09/18/2020 | Beckman Coulter Biomedical GmbH |
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