FDAFebruary 5, 2025device

DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137.

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

The hazard

the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high safety risk due to potential delays in patient results.

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulterbeckman

UPCs

15099590732103300116300117300123300124300128300139300141300145300160300164300166300179300181300183300188300195300197300207300209300250300258300259

Recall history

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

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