DermaRite recalls UltraSure Anti-Perspirant due to contamination risks from shared manufacturing facility. Affected lots produced before August 2027. Consumers should check NDC 61924-266-04.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
DermaRite is recalling UltraSure Anti-Perspirant and Deodorant products because they were made at a facility that contaminated other products. This means the product could contain harmful substances from the same manufacturing location.
The product was manufactured at a facility that previously had contamination issues. This means the product could contain harmful substances from the same facility that produced other contaminated items. However, the recall does not specify a direct health risk or injury mechanism.
People who own or use UltraSure Anti-Perspirant and Deodorant with NDC 61924-266-04 produced before August 2027. Those most at risk are individuals using the product regularly.
Check for the product name 'UltraSure Anti-Perspirant & Deodorant', NDC 61924-266-04, and production date before August 2027. The product comes in 118 mL (4 fl. oz.) containers.
Look for the NDC code 61924-266-04 and production date before August 2027 on the product label.
The recall does not specify that the product is unsafe; it indicates a potential contamination risk from the manufacturing facility.
The recall does not provide specific action steps for consumers, only product identification details.
Check for the NDC code 61924-266-04 and production date before August 2027 on the product label.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0177-2026 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0177-2026 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.
