DermaRite recalls 7.5 fl oz DermaSarra analgesic due to Burkholderia cepecia contamination. Stop using if you have the product with NDC 61924-189-08.
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
DermaRite is recalling its DermaSarra external analgesic product because it was contaminated with the bacteria Burkholderia cepecia. This contamination poses a risk of infection, especially for people with sensitive skin or open wounds.
The product was found to contain Burkholderia cepecia bacteria, which can cause infections. This contamination is particularly concerning for individuals with open wounds or compromised skin barriers.
People who own or use DermaSarra analgesic products with NDC 61924-189-08 are affected. Those with open wounds or sensitive skin may be at higher risk due to potential infection.
Check for the product name 'DermaSarra' with 7.5 fl oz (222 mL) per bottle. The NDC code is 61924-189-08 and the expiration date is February 2026.
If you have the recalled DermaSarra analgesic, stop using it immediately.
The product was found to be contaminated with Burkholderia cepecia bacteria, so it is not safe to use.
Stop using it immediately and contact DermaRite for further instructions.
Look for the NDC code 61924-189-08 on the product label, which expires February 2026.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0611-2025 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0611-2025 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.
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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.
