FDAJanuary 3, 2024device

Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137; in-vitro diagnostic instrument

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

The hazard

A software error caused an increase in tray gripper motion errors that causes intermittent hard stops and a delay in patient results.

What to do

FDA enforcement status: Completed

Brands named

beckman coulterbeckman

UPCs

15099590732103

Recall history

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

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Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137; in-vitro diagnostic instrument — Recall Details · AllClear