WhichRecall
Class IIReported 2025-05-28

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.

Recalled by CareFusion 213, LLC

Reason for Recall

Lack of Assurance of Sterility: The affected product may exhibit an open seal on the packaging of the applicator.

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Recall Number
D-0441-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-05-15
Reported
2025-05-28
Distribution
Nationwide in the U.S.
Code Info
Lot #s: 3354127 and 3350974, Exp Date: 12/31/2026
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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