Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K953084 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Access Ultrasensitive Insulin only used on the DxI 9000 Access Immunoassay Analyzer, Catalog Number ... | 2 | 02/05/2024 |
FEI # 2122870 Beckman Coulter, Inc. |
| Access Ultrasensitive Insulin Assay Kit, Part Number 33410. The product is a paramagnetic particle,... | 2 | 06/25/2008 |
FEI # 2050012 Beckman Coulter Inc |
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