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STA® - Staclot® dRVV Screen 2

DIAGNOSTICA STAGO · Model 00339 · UDI-DI 13607450003397

GIR Prescription
1
510(k) clearances
4
Adverse events
1
Recalls
12
Facilities

Recalls

DateFirmReason
2007-02-28American Diagnostica, Inc.Stability of product not assured. An increase of clotting time for both normal and abnormal plasmas

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.