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Anti-West Nile Virus ELISA (IgM)
EUROIMMUN Medizinische Labordiagnostika AG · Model EI 2662-9601 M · UDI-DI 04049016028185
1
510(k) clearances
5
Adverse events (2 deaths)
2
Recalls
9
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-10-03 | Focus Diagnostics Inc | The firm recalled due to higher reactivity with some samples in the effected lots, which may reflect a higher false positive rate. |
| 2008-10-08 | Inverness Medical | It has come to our attention that users of these product lots may experience an elevation in the rate of false positivity when compared with previous product lots. Internal qualit |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.