FDAMarch 10, 2020device

ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2, cK+, cNa+, cCa2+, cCl , cGlu, cLac, cCrea, ctBil, and co-oximetry parameters (ctHb, sO2, and the hemoglobin fractions FO2Hb, FCOHb, FMetHb, FHHb and FHbF) In vitro testing of sa...

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

The hazard

Analyzer's barcode reader misinterprets the contents of barcode label used for entering patient ID or accession number. The issue is related to barcode types not using a check digit. This could result in patient mixup or loss of sample resulting in delayed medical treatment

What to do

FDA enforcement status: Terminated

Brands named

radiometer medical apsradiometerradiometer medical

UPCs

05700693938011

Recall history

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

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