FDAJuly 30, 2018device

UniCel DxH 900 Coulter Cellular Analysis System, REF number C11478 Product Usage: Note: The DxH 900 hematology analyzer is CLIA categorized under document CR180294 and is currently marketed as a member of the instrument family of the DxH 800 cleared under K140911, per FDA s guidance, Guidance for...

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

The hazard

Complaints received of sporadic erroneously elevated platelet results without flags or system messages. Thrombocytopenia may go unrecognized.

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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