Pharmadel recalls Kingskin wart remover due to cGMP deviations. This affects specific lot numbers and expiration dates. Consumers should check their product details and contact Pharmadel for guidance.
cGMP deviations
Pharmadel is recalling Kingskin wart remover products due to manufacturing quality control issues. This recall affects specific lot numbers and expiration dates, but the products are not expected to cause serious harm if used properly.
The product was manufactured under cGMP deviations, which are quality control issues that could affect the product's safety and effectiveness. However, the recall does not indicate a risk of serious injury or death in normal use.
People who own or use Kingskin wart remover products with the specific lot numbers KSE-01 (expires Oct 2026) or KSE-02 (expires Feb 2027) are affected. Those using the product for wart removal are most at risk.
Check the product label for lot numbers KSE-01 (expires Oct 2026) or KSE-02 (expires Feb 2027). The product is distributed by Pharmadel in New Castle, DE.
Look for lot numbers KSE-01 (expires Oct 2026) or KSE-02 (expires Feb 2027) on the Kingskin wart remover product.
The recall is due to cGMP deviations, but the product is not expected to cause serious harm if used properly. Consumers should check the lot number and expiration date.
Check the product label for lot numbers KSE-01 (expires Oct 2026) or KSE-02 (expires Feb 2027). If you have these, contact Pharmadel for guidance.
The recall record does not specify a replacement option. Consumers should contact Pharmadel directly for further assistance.
We’ve drafted a message you can send Pharmadel to request your refund or repair — edit it as you like.
Subject: Recall D-0381-2025 — Pharmadel Pharmadel Hello, I own a Pharmadel that is covered by recall D-0381-2025 from Pharmadel. 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.
