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HemosIL dRVVT Screen
INSTRUMENTATION LABORATORY COMPANY · Model 00020301500 · UDI-DI 08426950513704
GIR
Prescription
1
510(k) clearances
4
Adverse events
1
Recalls
11
Facilities
Description
HemosIL dRVVT Screen
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-02-28 | American Diagnostica, Inc. | Stability of product not assured. An increase of clotting time for both normal and abnormal plasmas |
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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.