FDAOctober 23, 2025device

BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;

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

The hazard

The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used.

What to do

FDA enforcement status: Ongoing

Brands named

becton dickinsonbectonbecton dickinson

UPCs

30382902461006

Recall history

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

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