US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Apr 22, 2026 (4 months ago)

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of assurance of Sterility: potential product contamination

What was recalled

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26mL Applicators per carton. Carefusion 213 LLC, El Paso, TX 79912, NDC 54365-014-42.

Recalling firm
CareFusion 213, LLC
NDC code
54365-014-42
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0517-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Alcohol recalls

See all