FDADecember 19, 2016device

DxH 600 Coulter Cellular Analysis System, Catalog No. B23858

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

The hazard

Beckman Coulter has determined that additional clarification for the Blast Suspect messages is necessary. In rare situations, the UniCel DxH 800 and DxH 600 Coulter Cellular Analysis System may not flag or detect blasts in some blood samples. This is due to limitations in the available technology as well as sample limitations.

What to do

FDA enforcement status: Terminated

Brands named

beckman coulterbeckman

Recall history

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

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DxH 600 Coulter Cellular Analysis System, Catalog No. B23858 — Recall Details · AllClear