FDAFebruary 3, 2020device

ABL90 FLEX Analyzer, Model Numbers 393-090, with software versions below 3.4MR2 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting.

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

The hazard

The firm received reports of occurrences where the barcode reader misinterpreted the contents of a locally printed barcode label used for entering patient ID or accession number into the analyzer in connection with a sample measurement. This could result is patient mixup and/or lost of sample, resulting in delayed medical treatment.

What to do

FDA enforcement status: Terminated

Brands named

radiometer medical apsradiometerradiometer medical

Recall history

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

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ABL90 FLEX Analyzer, Model Numbers 393-090, with software versions below 3.4MR2 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting. — Recall Details · AllClear