Lower risk Drug recall · FDA · Published July 17, 2025

DermaRite PeriGiene Antiseptic Recall: Bacterial Contamination Risk

DermaRite recalls PeriGiene antiseptic bottles contaminated with Burkholderia cepecia bacteria. Products may pose infection risks if used. Consumers should check NDC numbers and expiration dates.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0613-2025Drug DermaRite ›

Lower-risk recall

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

Take action

Contact the company

Recalling firmDermaRite Industries, LLC7777 W Side Ave · North Bergen, NJ 07047-6436

✎ GovInfoNow plain-language explainer

DermaRite is recalling PeriGiene antiseptic products due to bacterial contamination. Using these products could lead to infections, especially for people with open wounds or compromised immune systems. Read more at govinfonow.com/recall/31976-dermarite-perigiene-antiseptic-recall-bacterial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/31976-dermarite-perigiene-antiseptic-recall-bacterial-contamination-risk · Updated August 17, 2026 · FDA enforcement record: FDA #D-0613-2025

Cite this page

“DermaRite PeriGiene Antiseptic Recall: Bacterial Contamination Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31976-dermarite-perigiene-antiseptic-recall-bacterial-contamination-risk. Based on FDA recall #D-0613-2025 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0613-2025%22&limit=1).

The FDA announced on July 17, 2025, that DermaRite Industries, LLC is recalling PeriGiene Health Care Antiseptic due to microbial contamination with Burkholderia cepacia. The recall affects 5,703 bottles distributed nationwide.

How to tell if you have it

Brand: DermaRite
Product: PeriGiene, Health Care Antiseptic (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle
NDC: 61924-198-08
Lot codes and expiration dates: 31013A (Exp. 11/2025); 40345A, 40355A (Exp. 4/2026); 40571A, 40580A (Exp. 6/2026); 40587A, 40591A (Exp. 7/2026); 40870.1, 40877.1 (Exp. 10/2026); 41093A (Exp. 12/2026); 50072A, 50079A (Exp. 1/2027)

The hazard

The products were found to be contaminated with the bacteria Burkholderia cepacia. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show DermaRite Industries, LLC has one other recall on record since August 27, 2025. On August 27, 2025, DermaRite issued a recall for Lantiseptic Skin Protectant due to CGMP deviation and contamination risk at the same facility. Other recent recalls of similar products include Blaine Labs Revitaderm Wound Gel Recall (April 8, 2026), Blaine Labs Revitaderm Gel Recall (April 8, 2026), and ProRx Semaglutide Injection Recall (October 15, 2025).

How to tell if you have this one

Check for NDC numbers 61924-198-08, 40345A, 40355A, 40571A, 40580A, 40587A, 40591A, 40870.1, 40877.1, 41093A, or 50072A. Products with expiration dates from 11/2025 to 1/2027 are affected.

Brand
DermaRite
Category
Drug

FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class I
Status
Ongoing
Distribution
Nationwide within the USA

Recall number	Product, codes & lots	Quantity
D-0610-2025	DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E (Chloroxylenol 0.2%), packaged in a) 800 ml (27 fl. oz.) bag-n-box (NDC 61924-092-27) and b) 1000ml (34 fl. oz.) bag-n-box (NDC 61924-092-34) , DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; Lot # and Expiration Date: a) 30550A, Exp. Date 7/2025; 30670A, 30682A, Exp. Date 8/2025; 40025A, Exp. Date 1/2026; 40375A, Exp. Date 4/2026; 40427A, 40436A, Exp. Date 5/2026; 50068A, Exp. Date 1/2027. b)30586A, 30586B, 30626A, Exp. Date 7/2025; 30628A, 30657A, Exp. Date 8/2025; 30741A, Exp. Date 7/2025; 30871A, Exp. Date 10/2025; 40002A, Exp. Date 12/2025; 40012A, Exp. Date 1/2026; 40301A, Exp. Date 3/2026; 40789 A, Exp. Date 9/2026; 50068B, Exp. Date 1/2027; 50144A, 50149A, Exp. Date 2/2027.	11,321 bag in boxes
D-0611-2025	DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08; Lot #: 40187.2, Exp. Date 2/2026	249 bottles
D-0612-2025	KleenFoam, Antimicrobial Foam Soap with Aloe Vera, (Chloroxylenol 0.5%) 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34; Lot #: 30705A, Exp. Date 8/2025; 30771A, Exp. Date 9/2025; 30920A, Exp. Date 10/2025; 40016A, Exp. Date 1/2026; 40303A, Exp. Date 4/2026; 40428A, Exp. Date 5/2026; 40505A, Exp. Date 6/2026; 41053C, 41053A, 41053B, Exp. Date 12/2026, 50017A, Exp. Date 1/2027.	6,973 cartridges
D-0613-2025	PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08; Lot #: 31013A, Exp. Date 11/2025; 40345A, 40355A, Exp. Date 4/2026; 40571A, 40580A, Exp. Date 6/2026; 40587A, 40591A, Exp. Date 7/2026; 40870.1, 40877.1, Exp. Date 10/2026; 41093A, Exp. Date 12/2026; 50072A, 50079A, Exp. Date 1/2027	5,703 bottles

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for NDC numbers and expiration dates listed in the recall notice to confirm if your product is affected.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Nationwide within the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 55 days after the firm started it.

Jul 17, 2025Firm started the recall
Sep 2, 2025FDA classified it Class I
Sep 10, 2025Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Is this product safe to use?

The recall states the product was contaminated with bacteria, so it is not safe to use. Consumers should stop using affected products.

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Keep exploring

Link to this recall

<a href="https://govinfonow.com/recall/31976-dermarite-perigiene-antiseptic-recall-bacterial-contamination-risk">DermaRite PeriGiene Antiseptic Recall: Bacterial Contamination Risk (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0613-2025 (July 17, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0613-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.