FDAApril 18, 2024device

DxI 9000 Access Immunoassay Analyzer, C11137; in-vitro diagnostic

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

The hazard

Beckman Coulter is recalling their DxI 9000 Access Immunoassay Analyzers, an in vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids, by correction. The reason for the recall is: Beckman Coulter has determined that the DxI 9000 Access Immunoassay analyzer accepts calibrator values scanned from multiple calibrator cards when an operator configures a new calibrator lot. The analyzer accepts the calibrator lot values from any scanned calibrator card, regardless of the assay test code or calibrator material lot number. The software is not validating the integrity of each calibrator barcode scanned to ensure they are all from the same calibrator card. This includes all software versions and all DxI 9000 instruments that are currently in the field. This issue does not impact calibrator material with 2D calibrator card barcodes. This may cause a failed calibration curve. The health risk

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulterbeckman

UPCs

15099590230623

Recall history

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

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