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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