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.
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
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.
The antiseptic products were found to contain Burkholderia cepecia bacteria. This contamination could lead to infections if the product comes into contact with open wounds or broken skin.
People using PeriGiene antiseptic for wound care or skin cleaning are at risk. Those with open wounds or weakened immune systems may face higher infection risks.
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.
Look for NDC numbers and expiration dates listed in the recall notice to confirm if your product is affected.
The recall states the product was contaminated with bacteria, so it is not safe to use. Consumers should stop using affected products.
The recall does not specify a remedy, so you should check with DermaRite directly for guidance.
Check the NDC numbers and expiration dates listed in the recall notice. Affected products have specific NDC codes and expiration dates from 11/2025 to 1/2027.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0613-2025 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0613-2025 from DermaRite. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
