Carefusion 213, Llc: 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. Ca...
Recall Summary BD PurPrep, a povidone-iodine and isopropyl alcohol skin preparation solution sold in 25-applicator cartons, is being recalled nationwide due to potential product contamination and lack of confirmed sterility. The product was distributed across all U.S. states and the District of Columbia. This is a Class II recall, meaning the product could cause temporary or reversible adverse health effects.
- Recalling firm
- 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
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-04-22
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide in the USA
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/55cc4c7d-b474-41b6-a40e-9d0877482151