FDAJuly 10, 2024device

DxC 500 AU Clinical Chemistry Analyzer, REF C63520 is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate reagents, calibrators, quality control (QC) material and other accessories. This system is for in vitro diagnostic use only.

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

The hazard

Due to a software issues, after the instrument processes 250 racks cumulatively, any subsequent racks with samples requiring rerun/reflex will be held in the Sample Handler's Buffer area and and error code "9000" will be reported. This issue may cause a delay of results.

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulter mishima k kbeckmanbeckman coulter

UPCs

14987666545065

Recall history

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

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