CareFusion 213, LLC recalls BD ChloraPrep Clear, 2% x/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin
Recalled May 28, 2025 · FDA recall D-0441-2025 · CareFusion 213
Hazard
Lack of Assurance of Sterility: The affected product may exhibit an open seal on the packaging of the applicator. · FDA Class II
Units
385,200 applicators
Sold at
Nationwide in the U.S.
Description
Lack of Assurance of Sterility: The affected product may exhibit an open seal on the packaging of the applicator.
Product
BD ChloraPrep Clear, 2% x/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, Applicator is sterile if package is intact, Flammable, External Use Only, 1 mL Applicator per pouch, 60 Applicators per inner carton, CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co., Made in the USA, Catalog Number 930480, NDC 54365-400-31.
Manufacturer(s)
CareFusion 213, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →