FDASeptember 21, 2017drug

Aplicare Povidone-Iodine Prep Pad, Antiseptic, Sterile Solution, Active Ingredient: Povidone-iodine USP 10%. Aplicare, INC., Meriden, CT 06450 USA. NDC: 52380-0111-1

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

The hazard

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

What to do

FDA enforcement status: Terminated

Brands named

medline

Recall history

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

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