Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K210127 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| iQ200 Series Urine Microscopy Analyzer: a) iQ 200 Select, Part Numbers C10684 and 700-3345; b) iQ 2... | 2 | 05/17/2023 | Beckman Coulter, Inc. |
| UA WIN 10 Kit, Catalog Number C52900, in-vitro diagnostic device, urine analysis | 2 | 05/17/2023 | Beckman Coulter, Inc. |
| DxU 840m Iris Urine Microscopy Analyzer, Catalog Number C76947, in-vitro diagnostic device, urine an... | 2 | 05/17/2023 | Beckman Coulter, Inc. |
| DxU 850m Iris Urine Microscopy Analyzer Catalog Number C49513, in-vitro diagnostic device, urine ana... | 2 | 05/17/2023 | Beckman Coulter, Inc. |
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