RecallHawk
Class II Recall

BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isopropyl alcohol (IPA), 70% v/v), 5.25 mL A

CareFusion 213, LLC

Summary

The FDA issued a Class II for BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isop by CareFusion 213, LLC. Reason: Lack of Assurance of Sterlity.

Details

Source

Drug Recall

External ID

D-0243-2026

Action Date

2026-01-07

Status

Ongoing

Category

drug

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

Lot/Code Info: Lot #: 5086623, Exp. Date 03/31/2028

Quantity Affected: 106,400 units

Reason for Recall

Lack of Assurance of Sterlity

Distribution

Nationwide within the United States

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-17

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 21 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

CareFusion 213, LLC has 6 FDA actions in our database, including 6 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (CareFusion 213, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does CareFusion 213, LLC have FDA actions?

CareFusion 213, LLC has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0243-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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