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, a povidone-iodine and isopropyl alcohol sterile solution used for skin preparation, is being recalled nationwide because the manufacturer cannot guarantee the product is sterile and it may be contaminated. The recall affects boxes containing 25 applicators of 0.36 fl. oz. each, distributed across all U.S. states and Washington, D.C. This is classified as a Class II recall, indicating a potential health risk.
- 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/a6075e16-eb25-45f9-afca-12f5eb5986ad