FDASeptember 13, 2018device

Abbott i-STAT CG8+ Cartridges intended for use in the in vitro quantification of potassium in arterial, venous, or capillary whole blood. List Number/UDI# : 03P88-25 ,(01)10054749000163(17)181028(10)L18059

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

The hazard

Inaccurate potassium results may be generated. When testing with control fluid and/or patient samples with low or reference range potassium concentration, elevated potassium results may be generated. When testing with samples with a high concentration of potassium, decreased potassium results may be generated

What to do

FDA enforcement status: Terminated

Brands named

abbott pointabbott

UPCs

10054749000163

Recall history

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

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