Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Non-Sterility: contamination of Aspergillus penicillioides, due to breach in package lidding.
What was recalled
BD ChloraPrep Clear 1mL Applicators, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, 0.03 fl. oz (1 mL) each, 60 Applicators per Carton, CareFusion 213, LLC, El Paso, TX 79912, Subsidiary of Becton, Dickinson and Co., REF 930480, NDC 54365-400-31.
Recalling firm
CareFusion 213, LLC
NDC code
54365-400-31
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0259-2025
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.