DermaRite recalls Lantiseptic skin protectant due to contamination at shared manufacturing facility. Products with NDC 61924-304-05 to 61924-304-12 may be affected. Stop using if expired by 08/2027.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
DermaRite is recalling Lantiseptic skin protectant products that were manufactured at a facility with contamination issues. This recall affects specific sizes and lot numbers that expired by August 2027. Using these products could expose you to contaminants from the shared facility.
The products were made at a facility that previously had contamination issues. This means the skin protectant could contain harmful substances from the shared manufacturing environment. However, the risk is low as the contamination is not specified as causing serious injury.
People who own or use Lantiseptic skin protectant products with the listed NDC numbers and expired by August 2027 are affected. Those with sensitive skin or using the product for medical purposes may be at higher risk.
Check the product label for the NDC numbers 61924-304-05, 61924-304-14, 61924-304-04, 61924-304-45, or 61924-304-12. Products with expiration dates on or before August 2027 are included in this recall.
Verify if your Lantiseptic product expires by August 2027 using the NDC numbers listed.
The products were manufactured at a facility that had previous contamination issues, so they may contain harmful substances.
Check if your product expires by August 2027 and has one of the listed NDC numbers. If so, stop using it and contact DermaRite for guidance.
The recall states a CGMP deviation but does not specify serious injury risks, so the risk is considered low.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0170-2026 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0170-2026 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.
