FDAJuly 12, 2024device

DxI 9000 Access Immunoassay Analyzer, catalog number C11137 in vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids

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

The hazard

Ground screws on Dxl 9000 PCB boards may cause electric shorts, leading to smoke and potentially delaying patient results. Smoke also poses a hazard to equipment and users.

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 in vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids — Recall Details · AllClear