FDANovember 18, 2022device

BECKMAN COULTER IRISpec CA/CB/CC control, REF 900-7211, For in vitro diagnostic use only.

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

The hazard

Beckman Coulter has become aware of an increase in customer complaints generated for intermittent IRISpec CB glucose control false positive results when used in conjunction with iChemVelocity Urine Chemistry Strips PN 800-7212

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulterbeckman

UPCs

10837461002611

Recall history

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

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