DermaRite Industries, LLC 2025-09-10 Health critical FDA
Health · FDA · Recall #FDA-D-0611-2025
DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle,… Recall
Issued September 10, 2025 · DermaRite Industries, LLC
In September 2025, DermaRite Industries, LLC recalled the DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle,…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
What you should do
- 1 Stop using DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact DermaRite Industries, LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- DermaRite Industries, LLC
- Category
- Health
- Recall date
- September 10, 2025
- Units affected
- Not reported
- Sold at
- Nationwide within the USA
- Recall number
- FDA-D-0611-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- DermaRite Industries, LLC has 11 recalls in our database, including 3 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.