Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K240252 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| UniCel DxH 690T COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C3452... | 2 | 09/17/2025 | Beckman Coulter Inc. |
| UniCel DxH 900 COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C11478 | 2 | 09/17/2025 | Beckman Coulter Inc. |
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