FDAJune 2, 2023device

Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly

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

The hazard

A software defect in the DxA Automation System may cause tests to be run on patient samples in tube types not compatible with the requested test, leading to erroneous patient results

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulter biomedicalbeckmanbeckman coulter

UPCs

15099590707118

Recall history

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

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