FDA Drugs recall ·
DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0611-2025
- Date
- (initiated July 17, 2025)
- Company / brand
- DermaRite Industries, LLC
7777 W Side Ave, North Bergen, NJ, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 249 bottles
- Hazard tags
- Sterility Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08
Why was it recalled?
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot #: 40187.2, Exp. Date 2/2026
Distribution
Nationwide within the USA
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0611-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.