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DermaRite Industries, LLC recalls DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Sid

Recalled September 10, 2025 · FDA recall D-0611-2025 · DermaRite Industries

Hazard
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia. · FDA Class I
Units
249 bottles
Sold at
Nationwide within the USA

Description

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

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
Manufacturer(s)
DermaRite Industries, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

DermaRite Industries, LLC recalls DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Sid | RecallWatchUSA