Skip to main content
Skip to recall details
Verified · FDAClass II — Possible RiskMedications

CHLORAPREP ONE-STEP BD ChloraPrep Scrub Teal, and 70% v/v isopropyl alcohol) Recall 2026

CHLORAPREP ONE-STEPIssued June 11, 2026Updated Reviewed by the Recall Watch editorial team

CHLORAPREP ONE-STEP BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 100 x 10.5 mL Applicators/case, NDC 54365-400-36, catalog number 930725NS; b) 100 x 10.5 m — recalled per FDA on 6/11/2026. 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.

Agency
FDA
Issued
Jun 11, 2026
Brand
CHLORAPREP ONE-STEP
Distribution
1 states
Lots affected
19
What to do right now

Steps to take for this recall

  1. Stop using it

    Take it out of rotation. Don't consume, wear, or operate.

  2. Verify the match

    Compare lot numbers, UPCs, and dates against your product.

  3. Return or dispose

    Follow the manufacturer's instructions to refund or safely dispose.

Verified summary of the official U.S. Food and Drug Administration notice · Issued June 11, 2026 · Last synced Nov 1, 2026

What's recalled

BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 100 x 10.5 mL Applicators/case, NDC 54365-400-36, catalog number 930725NS; b) 100 x 10.5 mL Applicators/case, bulk catalog number 930725NSB; STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co.

Available at AmazonAd
White first-aid box with bandages

Restock your medicine cabinet

First-aid kits, thermometers and OTC basics, searched on Amazon.

Shop at Amazon.com

Need it delivered? Start a free Amazon Prime trial.

Why it was recalled

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

Affected products & lot numbers
19 lots called out

Affected Lot Numbers

Check your product label — do not use if your lot number appears below.

Lot Number
Lot: a) 4157798
Exp 05/31/2027
5016842
Exp 12/31/2027
5112542
Exp 04/30/2028 b) 3330777
Exp 10/31/2026
3345111
Exp 12/31/2026
4037991
Exp 01/31/2027
4114505
Exp 04/30/2027
4156664
Exp 05/31/2027
4270441
Exp 09/30/2027
5078395
Exp 03/31/2028
Where was it sold
1 state

Distributed Nationwide in the USA

nationwide
Official noticefda.gov
More recalls like this
8 related — by brand, contaminant, and category

Frequently asked questions

Is the CHLORAPREP ONE-STEP recall still active?

Yes, this recall is currently active as of June 11, 2026. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: Lot: a) 4157798, Exp 05/31/2027, 5016842, Exp 12/31/2027, 5112542, Exp 04/30/2028 b) 3330777, Exp 10/31/2026, 3345111, Exp 12/31/2026, 4037991, Exp 01/31/2027, 4114505, Exp 04/30/2027, 4156664, Exp 05/31/2027, 4270441, Exp 09/30/2027, 5078395, Exp 03/31/2028. Check the label on your product.

What should I do if I have the recalled CHLORAPREP ONE-STEP?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.