FDAAugust 4, 2025device

DxC 500 AU Module w/ISE, DxC 500i, With ISE, REF: C63522 and DxC 500 AU Module, DxC 500i, Without ISE, REF: C6352; part of the DxC 500i Clinical Analyzer

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

The hazard

On a clinical analyzer, when ordering a Clinical Chemistry (CC) combination test simultaneously with an Immunoassay (IA) test, if the IA test is processed between the CC tests, CC sample status will remain In Progress with no errors, may cause processing delays.

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulterbeckman

UPCs

1498766654508914987666545072

Recall history

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

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