Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K060256 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| UniCel DxC Synchron Clinical Systems and UniCel DxC Synchron Access Integrated Clinical Systems T... | 2 | 07/22/2016 | Beckman Coulter Inc. |
| UniCel DxI 800 and 600 Access Immunoassay Systems, UniCel DxC 880i, 860i, 660i, and 680i SYNCHRON Ac... | 2 | 02/25/2010 | Beckman Coulter Inc. |
| UniCel® DxC 600/800 with Software v5.0.11, Part Number B12218. The UniCel® DxC Synchron® Clinica... | 2 | 10/24/2012 | Beckman Coulter Inc. |
| Unicel Closed Tube Aliquotter (UCTA) for UniCel DxC 660i, UniCel DxC 680i, UniCel DxC 860i, UniCel D... | 2 | 10/12/2012 | Beckman Coulter Inc. |
| Unicel DxC 600i System and Unicel Dxl 600 Access Immunoassay System | 2 | 09/21/2008 | Beckman Coulter Inc |
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