CareFusion 213, LLC recalls BD PurPrep
- Recalling company
- CareFusion 213, LLC
- Product
- 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.
- Reason
- Lack of assurance of Sterility: potential product contamination
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 22, 2026
- Reported
- May 13, 2026
- Distribution
- Nationwide in the USA
- Status
- Ongoing
- Lot / codes
- Lot# 4258309, 4260329, 4256875, Exp. Date, 08-31-2026; 4296453, 4317319, 4290654, Exp. Date 09-30-2026; 4322449, 4323861, 4318679, Exp Date 10-31- Exp.
- Company location
- El Paso, TX
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0517-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0517-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.