Is CareFusion 213, LLC recalled?

Yes — a recall has been published. 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

TemporaryFDAOngoing

Can cause harm that is usually temporary. Speak to your pharmacist or doctor — do not stop a prescribed medicine on your own.

BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol),500 x 1 mL applicators/case, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-31, bulk catalog number 930480NSB

Check the label for

Lot: 4088933, Exp 03/31/2027, 4177711, 4195438, Exp 06/30/2027, 5051114, Exp 02/29/2028, 5070540, Exp 03/31/2028, 5106254, Exp 04/30/2028, 5141607, Exp 05/31/2028, 5196494, Exp 07/31/2028.

Why: 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
Distributed: Distributed Nationwide in the USA
Company: CareFusion 213, LLC
Announced: 8 July 2026This is the date the recall was announced. A company may have started it weeks earlier.
Recall began: 11 June 2026

Already ate or took it and feel unwell? Call Poison Control — 1-800-222-1222

Source: FDA record D-0651-2026 · retrieved 29 June 2026

Read the official notice

Every recall is shown word for word from the FDA and USDA, with a link to the source.