CareFusion 213 Recalls BD ChloraPrep" Triple Swabsticks
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
CareFusion 213 Recalls BD ChloraPrep" Triple Swabsticks
CareFusion 213, LLC · Class II — Moderate Risk

Product Description
BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isopropyl alcohol (IPA), 70% v/v), 5.25 mL Applicator, CareFusion 213, LLC, El Paso, TX 79912, NDC 54365-401-29
Reason for Recall
Lack of Assurance of Sterlity
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
Nationwide within the United States
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA classified this recall as Class II, indicating the pharmaceutical product may cause temporary health problems or poses a slight threat of a serious nature. CareFusion 213, LLC initiated the recall on December 17, 2025 affecting 106,400 units. Lack of Assurance of Sterlity. The product was distributed nationwide. Consumers should check their purchases and discontinue use of any affected product. Contact CareFusion 213, LLC for further instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Other Injury Hazards and CareFusion recalls.