DermaRite Industries LLC Recalls

4 recalls found for DermaRite Industries LLC. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DRUG

6,973 KleenFoam Antimicrobial Foam Soap Cartridges Recalled for Contamination Risk

DermaRite Industries recalled 6,973 cartridges of KleenFoam Antimicrobial Foam Soap on July 17, 2025. The products are contaminated with the bacteria Burkholderia cepacia, which poses significant health risks. Consumers must stop using the soap immediately and contact DermaRite for guidance.

KleenFoam
Microbial Contamination
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Health & Personal Care
HIGH
FDA DRUG

PeriGiene Health Care Antiseptic Recalled for Burkholderia Contamination (2025)

Five thousand seven hundred three bottles recalled nationwide for microbial contamination with Burkholderia cepacia. DermaRite Industries LLC issued the recall on July 17, 2025. The product is PeriGiene Health Care Antiseptic, 222 mL bottles. Consumers should stop use and contact DermaRite for guidance.

PeriGiene
Microbial Contamination
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Health & Personal Care
HIGH
FDA DRUG

DermaSarra External Analgesic Recalled for Burkholderia Cepecia Contamination (DermaRite Industries)

DermaRite Industries recalled 249 bottles of DermaSarra External Analgesic on July 17, 2025 due to microbial contamination. The product, sold nationwide, carries NDC 61924-189-08 and Lot 40187.2 with an expiration date of February 2026. Consumers should stop using the product immediately and contact DermaRite for guidance.

DERMASARRA
Microbial Contamination
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Brand Statistics

Total Recalls
4
Pages
1