A major dermarite recall products alert has expanded significantly in September 2025, affecting over 32 personal care items distributed nationwide. The dermarite recall began with hand soaps in July but has grown to include sanitizers, moisturizers, shampoos, and various skin care products due to dangerous bacterial contamination. Understanding which dermarite products are affected and the health risks involved is crucial for American consumers who may have these items in their homes or healthcare facilities.
Understanding the DermaRite Industries Recall
The dermarite industries recall stems from contamination with Burkholderia cepacia complex (BCC), a group of bacteria that poses serious health risks, particularly to immunocompromised individuals. What started as a limited dermarite industries hand soap recall in July 2025 has expanded multiple times as testing revealed widespread contamination across the company’s product lines. The hand soap recall 2025 now encompasses a broad range of personal care and healthcare products sold in hospitals, nursing homes, and retail stores across America.
Complete DermaRite Recall List
The dermarite recall list includes 32 different products spanning multiple categories. Here’s the comprehensive breakdown of recalled items:
Personal Care and Cleansing Products
| Product Name | Product Type | Primary Use |
| 3-N-1 Body Wash and Shampoo | Multi-purpose cleanser | Body and hair washing |
| 4-N-1 Wash Cream | No-rinse wash cream | Skin cleansing without water |
| Clean-N-Free | Body wash and shampoo | Rinse-free cleaning |
| DermaRain | Body wash and shampoo | General bathing |
| Renew Hair and Body Wash | Dual-purpose cleanser | Hair and body care |
| TotalBath | Body wash and shampoo | Complete body cleaning |
| WhirlBath | Body wash and shampoo | Therapeutic bathing |
Hand Sanitizers and Antiseptic Products
| Product Name | Product Type | Primary Use |
| DermaKleen | Healthcare antiseptic lotion | Hand sanitizing in medical settings |
| Gel Rite | Gel hand sanitizer | Hand disinfection |
| Hand E Foam | Foaming hand sanitizer | Hand hygiene |
| KleenFoam | Antimicrobial foam soap | Hand washing and sanitizing |
| San-E-Foam | Hand sanitizer | Hand disinfection |
Skin Care and Treatment Products
| Product Name | Product Type | Primary Use |
| DermaCerin | Moisturizing cream | Skin protection and hydration |
| DermaDaily | Moisturizing lotion | Daily skin care |
| DermaFungal | Antifungal cream | Treating fungal infections |
| DermaMed | Skin protectant | Wound and skin protection |
| DermaSarra | External analgesic | Pain relief for skin irritation |
| DermaVantage | Moisturizing lotion | Advanced skin care |
The complete dermarite product recall affects products distributed throughout the United States and Puerto Rico.
Health Risks and Safety Concerns
The bacterial contamination poses varying levels of risk depending on individual health status. For healthy individuals with minor cuts or skin lesions, exposure may result in localized skin infections. However, the primary concern involves immunocompromised patients, including those with chronic illnesses, elderly individuals, and anyone receiving medical care. In these vulnerable populations, Burkholderia cepacia can enter the bloodstream and cause life-threatening sepsis.
Healthcare facilities using these products face particularly serious risks, as many patients in hospitals and nursing homes have compromised immune systems. The bacteria can survive in aqueous solutions and resist many common preservatives, making contamination especially dangerous in medical settings.
Timeline of the Expanding Recall
The dermarite recall has evolved significantly since its initial announcement:
July 16, 2025: Initial Recall
DermaRite first announced a limited recall of four hand soap products after bacterial contamination was detected during routine testing.
August 8, 2025: First Expansion
The company expanded the recall to include additional hand soap varieties and some personal care products, bringing the total to 16 items.
August 27, 2025: Major Expansion
A significant expansion added moisturizers, antifungal creams, and body washes to the recall list.
September 2025: Current Status
The recall now encompasses 32 different products across multiple categories, making it one of the largest personal care product recalls of 2025.
What Consumers Should Do Immediately
If you have any dermarite recall products in your home or workplace, take these immediate steps:
Check Your Products
Compare any DermaRite products you own against the complete recall list. Pay special attention to lot numbers and expiration dates, as specific batches are affected.
Stop Using Immediately
Discontinue use of any recalled products immediately, especially if you or someone in your household has a compromised immune system, chronic illness, or open wounds.
Proper Disposal
Dispose of recalled products according to your local hazardous waste guidelines. Do not pour liquid products down drains, as this could create environmental contamination.
Seek Medical Attention
Contact your healthcare provider if you’ve used recalled products and experience symptoms such as skin infections, fever, fatigue, or unusual skin irritation.
Where DermaRite Products Were Sold
Dermarite products were widely distributed through multiple channels:
- Major retailers including Amazon, Target, and Walmart
- Healthcare supply companies
- Hospitals and medical facilities
- Nursing homes and long-term care facilities
- Independent pharmacies and medical supply stores
Products were sold nationwide and in Puerto Rico, making the potential exposure significant.
Company Response and Contact Information
DermaRite Industries has acknowledged the severity of the situation and is working with the FDA to address the contamination. The company has established dedicated recall support:
Consumer Hotline: 888-943-5190 (Monday-Friday, 8:00 AM – 5:00 PM EST)
Email: dermarite5186@sedgwick.com
The company has also confirmed that their wound care and nutritional products are not affected by this recall and remain safe for use.
FDA Investigation and Industry Impact
The FDA is conducting a comprehensive investigation into DermaRite’s manufacturing practices. This recall highlights ongoing concerns about Burkholderia cepacia contamination in pharmaceutical and personal care products. According to FDA data, B. cepacia has been responsible for an increasing percentage of non-sterile product recalls, rising from 22% between 1998-2006 to 39% by 2012.
The investigation focuses on:
- Water system contamination in manufacturing
- Inadequate preservative systems
- Poor manufacturing practices
- Quality control failures
Prevention and Future Safety Measures
This recall underscores the importance of robust manufacturing standards for personal care products. Consumers should:
- Choose products from companies with strong quality control records
- Report adverse reactions to the FDA’s MedWatch program
- Stay informed about product recalls through FDA alerts
- Be especially cautious with products used in healthcare settings
Alternative Products and Recommendations
While the recall is being resolved, consumers need safe alternatives for personal care and sanitization. The FDA recommends choosing products from established manufacturers with good safety records. For healthcare facilities, switching to approved alternatives that don’t contain the contaminated ingredients is crucial for patient safety.
Long-term Implications for the Industry
This extensive dermarite recall may lead to stricter FDA oversight of personal care product manufacturing, particularly for products used in healthcare settings. The agency has already issued guidance warning manufacturers about Burkholderia cepacia risks in water-based products.
FAQ
What products are included in the DermaRite recall?
The dermarite recall list includes 32 products spanning hand sanitizers, body washes, moisturizers, antifungal creams, and various personal care items contaminated with Burkholderia cepacia bacteria.
Why were DermaRite products recalled?
Dermarite products were recalled due to contamination with Burkholderia cepacia complex, bacteria that can cause serious infections, particularly in immunocompromised individuals.
What should I do if I have recalled DermaRite products?
Stop using any dermarite recall products immediately, dispose of them safely, and contact your healthcare provider if you’ve experienced any adverse reactions after use.
Is the hand soap recall still expanding in 2025?
Yes, the hand soap recall 2025 has expanded multiple times since July, growing from 4 initial products to 32 different items as of September 2025.
Where can I get more information about the DermaRite recall?
Contact the dermarite industries recall hotline at 888-943-5190 or email dermarite5186@sedgwick.com for specific questions about recalled products.
Are all DermaRite products recalled?
No, the dermarite product recall specifically affects personal care items. The company’s wound care and nutritional products are not part of this recall.
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