FDAMay 7, 2025device

DxI 9000 Access Immunoassay Analyzer C11137

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

The hazard

Analyzer has calibration issues where curves switched from passed to failed due to system errors during aspiration. This anomaly causes erroneous results and delays if unnoticed. RLU values may be misinterpreted as valid measurements by LIS.

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 C11137 — Recall Details · AllClear