FDAJuly 24, 2018device

Diagnostica Stago STA N¿oplastine¿ CI Plus, 10 ml vial. In-Vitro Diagnostic for determination of the prothrombin time (PT) in plasma. (REF 00667) The STA¿ - N¿oplastine¿ CI Plus kits provide reagents for the determination of the prothrombin time (PT) in plasma with STA-R¿, STA Compact¿ and STA Sa...

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

250791201807310360745000667425079220180731250911201808312512312018103125131120181130251364201811302514272018113025152820181231251707201901312517082019013125176720190228

Recall history

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

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Diagnostica Stago STA N¿oplastine¿ CI Plus, 10 ml vial. In-Vitro Diagnostic for determination of the prothrombin time (PT) in plasma. (REF 00667) The STA¿ - N¿oplastine¿ CI Plus kits provide reagents for the determination of the prothrombin time (PT) in plasma with STA-R¿, STA Compact¿ and STA Sa... — Recall Details · AllClear