FDAApril 26, 2022device

TEG 5000 Functional Fibrinogen Reagent, Item No. 07-034

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

The hazard

Due to a shift in the citrated blood reference range for a normal population, the ranges stated in the IFU are changing. If the clinician relies solely on affected results in comparison to the normal donor reference range, it could lead to misdiagnosis and incorrect treatment or failure to treat.

What to do

FDA enforcement status: Terminated

Brands named

haemonetics

UPCs

20812747018095

Recall history

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

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