FDAAugust 21, 2017device

AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer is intended for use as an in vitro diagnostic device for immunophenotyping.

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

The hazard

Beckman Coulter has identified that an incorrect setting using a proprietary software configuration tool can result in the Sample Prep Probe of the AQUIOS CL drawing aspirant from the wrong tube in a cassette which manifests in incorrect values being reported out of the laboratory for some patient samples.

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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