FDAMarch 2, 2018device

BD MAX DNA MMK Lab Use, catalog no. 442828

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

The hazard

The package insert incorrectly lists the volume of the primer and probe diluent to use for the reconstitution of the master mix tube. Adding the incorrect amount of diluent could have an effect on the assay.

What to do

FDA enforcement status: Terminated

Brands named

becton dickinsonbectonbecton dickinson

Recall history

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

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