Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K982485 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CMV IgM EIA, in vitro diagnostic. | 2 | 12/06/2022 | Bio-Rad Laboratories, Inc. |
| SeraQuest***CMV IgM TEST SET For the detection of CMV IgM Antibodies 96 Test Set Cat. No. 01-150 Sto... | 3 | 01/23/2012 | Quest International, Inc. |
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