Carefusion 213, Llc: Bd Chloraprep Clear, (2% W/v Chlorhexidine Gluconate (chg) And 70% V/v Isopropyl Alcohol),500 X

Recall Summary BD ChloraPrep CLear skin antiseptic applicators (500 x 1 mL cases) have been recalled nationwide because they were distributed without proper sterilization assurance. The products were intended to be sterilized before customer use but were shipped directly to customers instead. This recall affects healthcare facilities and other users across all U.S. states and territories.

Recalling firm
CareFusion 213, LLC
Product
BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol),500 x 1 mL applicators/case, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-31, bulk catalog number 930480NSB
Reason
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
Classification
Class II
Category
drug recall
Country
United States
Agency
U.S. Food and Drug Administration
Recall date
2026-06-11
Status
Ongoing
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
Distributed Nationwide in the USA

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/eb42d373-d667-4e3a-9f93-c51a7b342e09