CareFusion 213, LLC: BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine
Recall 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. Recalled by CareFusion 213, LLC. Distribution: Distributed Nationwide in the USA. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot: a) 3194046, Exp. 06/30/2026, 3217036, Exp 07/31/2026, 3279434, Exp 09/30/2026, 3286268, 3304460, Exp 10/31/2026, 3. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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