FDAApril 23, 2025device

DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software version 1.20

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

The hazard

A new software update (v1.20) is introducing error codes for the Dxl 9000 which prevents the assay from being performed and a delay in results from being generated, and may require field service to resolve the delay.

What to do

FDA enforcement status: Ongoing

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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DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software version 1.20 — Recall Details · AllClear