DermaRite recalls Renew Skin Repair Cream (5g and 4oz tubes) due to contamination risk from shared manufacturing facility. Consumers should check product labels for NDC codes 61924-405-05 or 61924-405-04.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
DermaRite is recalling Renew Skin Repair Cream tubes that were made at a facility where contamination occurred. This could mean the product contains harmful substances that might cause health issues if used.
The cream was manufactured at a facility that previously had contamination issues. This means the product might contain harmful substances that could cause health problems if used, though the specific contaminants are not identified.
People who own or use Renew Skin Repair Cream tubes with NDC codes 61924-405-05 (5g) or 61924-405-04 (4oz) are affected. Those with sensitive skin or allergies may be at higher risk.
Check the product label for NDC codes 61924-405-05 (5g tube) or 61924-405-04 (4oz tube). The recall covers all lots up to expiration date 08/2027.
Look for NDC codes 61924-405-05 or 61924-405-04 on the tube packaging.
The recall states there is a risk of contamination from the manufacturing facility, but specific harmful substances are not identified. The product may be safe for most users, but the recall recommends checking the label.
The recall does not specify a remedy, so you should check the product label for the NDC codes and contact DermaRite if you have concerns.
The recall only covers Renew Skin Repair Cream tubes with the specific NDC codes mentioned. Other products are not included.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0175-2026 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0175-2026 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.
