FDANovember 8, 2024device

Access Intact PTH assay on the DxI 9000 Access Immunoassay Analyzer, Catalog number A16972, for the quantitative determination of intact parathyroid hormone (parathyrin, PTH) levels in human serum and plasma.

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

The hazard

The reason for the recall is that EDTA and lithium heparin plasma samples that are stored in the DxI 9000 Access Immunoassay Analyzer sample wheel for a prolonged period before performing the intact PTH (parathyroid hormone) test may produce falsely decreased intact parathyroid hormone results. This could lead to a missed diagnosis, a delay in treatment, or inappropriate clinical management, depending upon the patient s clinical condition.

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulterbeckman

UPCs

15099590201937

Recall history

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

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