DermaRite Recall 2025: Expanded Product List & Safety Guide
DermaRite Recall: Essential Guide to the 2025 Product Expansion and Safety Steps
The DermaRite recall has significantly expanded, now encompassing over 32 personal care and medical products due to dangerous bacterial contamination . This voluntary action, initiated in July 2025 and broadened in late August, targets potential Burkholderia cepacia contamination across hand soaps, sanitizers, cleansers, and moisturizers . Consequently, consumers and healthcare facilities nationwide must immediately check their inventories.
Understanding the scope of this skincare product recall is crucial for safety. This contamination poses severe risks, especially for immunocompromised individuals or those with chronic health conditions. This guide provides a clear breakdown of affected items, health risks, and actionable steps to ensure your safety. Stay informed and protect your household from potential harm.
Why Did DermaRite Expand This Recall?
DermaRite Industries expanded its initial voluntary recall out of an abundance of caution after identifying potential microbial contamination. The company discovered that Burkholderia cepacia complex (Bcc), a group of bacteria, contaminated certain products. This contamination occurred during manufacturing, affecting numerous lots distributed across the United States and Puerto Rico.
To date, DermaRite has not received any reports of adverse events related to this contamination. However, the company acted proactively to prevent possible infections. Their commitment to transparency and customer safety drove this significant expansion, which now includes 32 products, from antiseptic soaps to skin protectants.
Comprehensive List of Recalled DermaRite Products
The DermaRite recall affects a wide array of products. Notably, these include rinse-free cleansers, moisturizing lotions, antiseptic soaps, and hand sanitizers. All recalled items have expiration dates on or before August 2027.
For clarity, here is a table of some key recalled products and their uses:
| Product Name | Type | Intended Use |
| DermaKleen | Antiseptic Lotion Soap | Handwashing to reduce bacteria |
| DermaSarra | External Analgesic | Temporary itch relief from minor skin irritations |
| KleenFoam | Antimicrobial Foam Soap | Handwashing after caregiving or diaper changes |
| PeriGiene | Antiseptic Cleanser | Perineal area cleansing |
| DermaCerin | Moisturizing Cream | Protect and relieve dry, chapped skin |
| Gel Rite | Instant Gel Hand Sanitizer | Decrease bacteria on skin |
| Renew Dimethicone | Skin Protectant | Treat and prevent diaper rash |
For a complete list of all 32 recalled products, including item numbers and lot numbers, refer to the official FDA recall announcement or DermaRite’s website.
Health Risks: Understanding Burkholderia Cepacia Contamination
What is Burkholderia Cepacia?
Burkholderia cepacia complex (Bcc) is a group of bacteria commonly found in soil and water. While it often poses minimal risk to healthy individuals, it can cause severe, life-threatening infections in certain populations.
Who is Most at Risk?
Immunocompromised individuals face the greatest danger. This includes people with cystic fibrosis, chronic lung diseases, or weakened immune systems from conditions like cancer or transplants. For these vulnerable groups, Bcc infections can lead to pneumonia, bloodstream infections (sepsis), and other serious complications.
Healthy individuals with minor skin lesions may experience local infections, such as skin rashes or irritation. However, the bacteria can spread rapidly in immunocompromised persons, leading to systemic infections that are difficult to treat due to significant antibiotic resistance.
Symptoms of a Burkholderia Cepacia Infection
Recognizing the symptoms of a Bcc infection is critical for seeking prompt medical attention. Consequently, watch for these signs:
- Respiratory issues: Difficulty breathing, coughing, or congestion
- Fever and fatigue: Unexplained fever or extreme tiredness
- Skin reactions: Localized redness, swelling, or pus at the site of a minor lesion
If you or someone in your care experiences these symptoms after using a recalled product, contact a healthcare provider immediately. Moreover, report any adverse reactions to the FDA’s MedWatch program.
What Should Consumers Do Immediately?
1. Check Your Products
Identify any DermaRite products in your home or facility. Cross-reference them with the official recalled product list provided by DermaRite or the FDA. Pay close attention to the item numbers, lot numbers, and expiration dates.
2. Stop Using Recalled Items
Immediately discontinue use of any recalled product. Furthermore, ensure that caregivers, family members, and patients are aware of the recall to prevent accidental use.
3. Destroy and Dispose
Destroy the recalled products in accordance with your facility’s guidelines or household disposal methods. DermaRite has instructed distributors and customers to eliminate these items safely.
4. Contact Healthcare Providers if Needed
If you have used a recalled product and experience symptoms, consult your physician or healthcare provider without delay. This is especially crucial for immunocompromised individuals.
5. Report Adverse Events
Report any quality problems or adverse reactions to the FDA’s MedWatch Adverse Event Reporting program. You can submit reports online at www.fda.gov/medwatch/report.htm or via mail/fax .
DermaRite’s Response and Customer Support
DermaRite Industries has expressed regret for any inconvenience caused by this recall. In a statement dated September 8, 2025, the company emphasized its dedication to “acting quickly, transparently, and responsibly” to maintain high standards of care.
The company is actively working to restore full product availability. Importantly, they confirm that their wound care and nutritional products are not part of this recall and remain safe for use.
For questions or further information, consumers can contact DermaRite’s representative:
- Phone: Sedgwick at 888-943-5190 (Mon-Fri, 8 AM–5 PM EST)
- Email: dermarite5186@sedgwick.com
Conclusion: Prioritize Safety and Stay Informed
The expanded DermaRite recall underscores the importance of vigilance in product safety. By immediately checking your products, discontinuing use of recalled items, and following disposal guidelines, you protect yourself and your loved ones from potential harm.
Stay updated on this developing situation by regularly checking the FDA’s recall page or DermaRite’s official website. Your health and safety are paramount—act now to ensure a risk-free environment.
Check your products today and share this critical recall information with your community to safeguard everyone’s health.
FAQs About the DermaRite Recall
1. What caused the DermaRite recall?
The recall was initiated due to potential contamination with Burkholderia cepacia complex (Bcc), bacteria that can cause serious infections, particularly in immunocompromised individuals.
2. Are all DermaRite products recalled?
No. Only specific lots of 32 personal care and medical products are recalled. DermaRite’s wound care and nutritional products are not affected and remain safe for use.
3. What should I do if I used a recalled product?
Discontinue use immediately. Destroy the product. If you experience symptoms like fever, respiratory issues, or skin infections, contact your healthcare provider promptly.
4. How can I get a refund or replacement?
Contact DermaRite’s representative, Sedgwick, at 888-943-5190 or email dermarite5186@sedgwick.com for instructions on refunds or replacements.
5. Where can I find the complete list of recalled products?
The full list, including product descriptions, item numbers, and lot numbers, is available on the FDA’s official recall announcement and DermaRite’s website.
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