FDAOctober 25, 2017device

Neoplastine¿ Cl Plus ¿ (ref. 00375) Product Usage: Manual or automated determination of the prothrombin time (PT).

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

The hazard

Confirmed defect of homogeneity where some reagent vials will give prolonged Prothrombin Time (decreased PT%).

What to do

FDA enforcement status: Terminated

Brands named

diagnostica stagodiagnostica

Recall history

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

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