HIGHFDA DRUG

BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 25 x 26 mL applicators/case, NDC 54365-400-39, catalog number 930825NS, b) 50 x 26 mL...

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

CHLORAPREP ONE-STEPCareFusion 213, LLCHealth & Personal CareDrugs & MedicationsLot: a) 3352149Exp 12/31/2026 b) 5028798Exp 01/31/2028

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
June 11, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
June 11, 2026
Hazard Level
HIGH
Brands
CHLORAPREP ONE-STEP, CareFusion 213, LLC
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
CHLORAPREP ONE-STEP, CareFusion 213, LLC
Model numbers
Lot: a) 3352149, Exp 12/31/2026 b) 5028798, Exp 01/31/2028, 5069651, Exp 03/31/2028.
UPC codes
54365-400, 54365-400-39
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    June 11, 2026

  2. Reported by FDA DRUG

    July 8, 2026

  3. RecallRadar source check

    July 14, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact CareFusion 213, LLC or your healthcare provider for guidance. Notification method: Letter

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Full Description

BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 25 x 26 mL applicators/case, NDC 54365-400-39, catalog number 930825NS, b) 50 x 26 mL applicators/case, NDC 54365-400-39, bulk catalog number 930825NSB; STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co.. Generic: CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL; Brand: CHLORAPREP ONE-STEP. 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. Classification: Class II. Quantity: 125 units. Distribution: Distributed Nationwide in the USA

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Lot: a) 3352149
Exp 12/31/2026 b) 5028798
Exp 01/31/2028
5069651
Exp 03/31/2028.
UPC Codes
54365-400
54365-400-39
Affected States
ALL
Report Date
July 8, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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