Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K093955 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Elecsys Anti-HAV IgM assay-for the in vitro qualitative detection of IgM antibodies to hepatitis A v... | 2 | 12/12/2019 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
| Anti-HAV IgM test System, Material No. 11820591160 Product Usage: The Roche Elecsys Anti-HAV IgM... | 2 | 01/29/2019 |
FEI # 1823260 Roche Diagnostics Corporation |
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