Carefusion 213, Llc: Bd Chloraprep Clear, (2% W/v Chlorhexidine Gluconate (chg), And 70% V/v Isopropyl Alcohol (ipa), Packaged As A) 100 X

Recall Summary BD ChloraPrep Clear skin antiseptic applicators (in 100 or 250-count cases) are being recalled because unsterilized products intended for further processing were accidentally distributed to customers nationwide. The affected products may not be sterile and were meant to be sterilized before use.

Recalling firm
CareFusion 213, LLC
Product
BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG), and 70% v/v isopropyl alcohol (IPA), Packaged as a) 100 x 3ml applicators/case, NDC 54365-400-32, catalog 930400NS; b) 250 x 3ml applicators/case, NDC 54365-400-32, bulk Catalog 930500NSB, Sterile Solution, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co.
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/644ad5f0-62fd-4847-9322-964e245b8be4