FDAApril 24, 2017device

UniCel DxH 600 Coulter Cellular Analysis System, Catalog No. B23858.

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

The hazard

There is a possibility of a data acquisition disruption that may cause an unusual light scatter event pattern for the white blood cell differential that may not have a system flag and/or message. The events associated with the unusual light scatter pattern may be incorrectly removed from analysis which can result in an erroneous differential result.

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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