Dermarite Industries, LLC — DermaSarra recall — Check with your pharmacist

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Dermarite Industries, LLC

Check with your pharmacist

Do not stop taking a prescribed medicine on your own — ask your pharmacist for a replacement pack today.

Class I

The FDA’s most serious category — a reasonable probability of serious harm or death.
Refunds don't require a receipt, and you don't need proof of purchase.
FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14

Check with your pharmacist Filed 2025-09-10

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

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

Check these codes: Lot #: 40187.2, Exp. Date 2/2026

249 bottles · distributed nationwide within the usa Recall D-0611-2025 on FDA.gov ↗

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