FDAJuly 24, 2018device

Diagnostica Stago STA N¿oplastine¿ CI, 10 ml vial. In-Vitro Diagnostic for determination of the prothrombin time (PT) in plasma. REF: 00666 The STA¿ - N¿oplastine¿ CI kits provide reagents for the determination of the prothrombin time (PT) in plasma with STA-R¿, STA Compact¿ and STA Satellite¿. (...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

QC values outside of the assigned ranges (prolonged Prothrombin time / decreased PT %)

What to do

FDA enforcement status: Terminated

Brands named

diagnostica stagodiagnostica

UPCs

251426201811300360745000666725176320190228

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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