FDASeptember 6, 2016device

AQUIOS CL Flow Cytometer, Catalog No. B30166; Intended for use with in vitro diagnostic flow cytometry applications using up to four florescent detection channels.

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

The hazard

Beckman Coulter is recalling the AQUIOS CL System because the use of the reagent carousel can lead to misalignment of the carousel and damage to the prep probe.

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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