FDAMay 22, 2024device

Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Catalog #C11137.

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

The hazard

The reason for this recall is Beckman Coulter has determined that when a DxI 9000 Access Immunoassay Analyzer is connected to a Laboratory Automation System (LAS); is running with the software versions 1.17 and below; and a sample tube is sent from the LAS to DxI 9000 Access Immunoassay Analyzer, an out of sequence message will be sent from the Analyzer to the LAS. This issue may result in multiple error messages (i.e., a sample pick and place (PnP) error or a no result obtained (NRT) flag may be displayed) and subsequently a risk of delays in processing/reporting patient test results and patient treatment.

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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Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Catalog #C11137. — Recall Details · AllClear