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FDAOctober 4, 2019device

Randox Liquid Cardiac Controls Catalogue Number CQ5052.

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

The hazard

Removal of claims for N-proBNP in the Liquid Cardiac Control catalogue number CQ5052 due to an observed decrease in recovery for N-Terminal Pro-Brain Natriuretic Peptide (NT-proBNP) in recent lots.

What to do

FDA enforcement status: Terminated

Brands named

randox laboratoriesrandox

UPCs

05055273207453

Recall history

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

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