Carefusion 213, Llc: 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
Recall Summary BD PurPrep Povidone-iodine Sterile Solution (0.36 fl. oz. applicators) is being recalled nationwide because the manufacturer cannot guarantee the product is sterile and it may be contaminated. The product is used as a skin antiseptic before medical procedures. This is a Class II recall, meaning use of the product could cause serious adverse health effects or death.
- 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, 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
- 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/cefc49fd-b523-45c2-a771-c3725c987903