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FDAFDA · Food and drugs·Recall number D-0518-2026

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 fl. oz. (10.5 mL) x 25 applicators per box. Carefusion 213, LLC, El Paso, TX 79912, subsidary of Becton Dickinson and Co. NDC 54365-014-41

Published May 13, 2026 · Recall initiated: April 22, 2026

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Lack of assurance of Sterility: potential product contamination

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
PURPREP
Manufacturer
CareFusion 213, LLC
Distributor
Nationwide in the USA
Lot
Lots# 4263873, Exp. Date 08-31-2026, 4320590, Exp. Date 09-30-2026, 4320591, Exp. Date 10-31-2026.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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