Warning
CareFusion 213 Recalls BD ChloraPrep Clear
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0690-2026Drug / Pharmaceutical
CareFusion 213 Recalls BD ChloraPrep Clear
CareFusion 213, LLC · Class II — Moderate Risk
Product Description
BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL applicators/carton, 0.03fl oz (1 mL) each, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-31
Reason for Recall
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
U.S.A. Nationwide
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A Class II FDA recall has been issued for a pharmaceutical product from CareFusion 213, LLC, initiated on July 9, 2026. Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator. This recall covers 43,066,599 units, distributed in U.S.A. Nationwide. While not the highest severity, consumers should exercise caution and stop using the product until the recall is resolved.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects and CareFusion recalls.