Medical Device Recalls
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11 to 17 of 17 Results
510(K) Number: K140911 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B66445, B68304,... | 2 | 05/24/2017 | Beckman Coulter Inc. |
UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B68304 | 2 | 01/11/2017 | Beckman Coulter Inc. |
UniCel DxH 600 Coulter Cellular Analysis System, Software Version 3.0.2.0, Part No. 775222 The UniC... | 2 | 12/16/2015 | Beckman Coulter Inc. |
UniCel DxH 600 Coulter Cellular Analysis System, Software Version 1.1.1.0, Part No. B23858 The DxH ... | 2 | 12/16/2015 | Beckman Coulter Inc. |
UniCel DxH 600 Coulter Cellular Analysis System, REF number B23858. Product Usage: Note: The DxH... | 1 | 05/23/2019 | Beckman Coulter Inc. |
UniCel DxH 600 Coulter Cellular Analysis System, Catalog No. B23858. | 2 | 05/24/2017 | Beckman Coulter Inc. |
DxH 600 Coulter Cellular Analysis System, Catalog No. B23858 | 2 | 01/11/2017 | Beckman Coulter Inc. |
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