RecallRadar
ModerateReported January 7, 2026

BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG)

Recalled by CareFusion 213, LLC

Product image for 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
Product image via DailyMed (National Library of Medicine). It may show general packaging and not the exact recalled lot — always confirm using the codes below.

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

CareFusion 213, LLC has recalled BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on January 7, 2026 and was initiated on December 17, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), with approximately 106,400 units affected. The company behind the recall is CareFusion 213, LLC, based in El Paso, TX. The FDA describes the product as: “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”

Why was BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG) recalled?

According to the FDA, the stated reason for the recall is: “Lack of Assurance of Sterlity.”

What should you do?

If you think you may have bought BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), compare it against the product description and identifying codes (Lot #: 5086623, Exp. Date 03/31/2028) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact CareFusion 213, LLC or your local health authority.

About this recall

This recall was distributed in TX. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
January 7, 2026
Recall started
December 17, 2025
Distributed in
TX
What was recalled
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
Why it was recalled (as stated by the FDA)
Lack of Assurance of Sterlity
How to identify the affected product
Lot #: 5086623, Exp. Date 03/31/2028
Amount recalled
106,400 units

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG) recalled?+

According to the FDA: Lack of Assurance of Sterlity

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG)?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: D-0243-2026. Information last synced from the FDA on July 5, 2026.

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