Edge Pharma recalls multiple batches of Cantharidin PLUS and Cantharidin/Salicylic Acid Gel-Forming Suspension for potential quality issues. Consumers should check product labels for NDC 05446-0970-03 and affected dates.
CGMP Deviations
Edge Pharma is recalling certain topical cantharidin products due to manufacturing quality control issues. This recall affects products that may not meet safety standards, though no injuries have been reported.
CGMP deviations refer to failures in the manufacturing process that could lead to products not meeting safety and quality standards. This means the recalled products might contain impurities or be inconsistent in strength, potentially causing adverse reactions.
People who own or use the recalled cantharidin topical products are affected. Those with sensitive skin or using the products for medical purposes may be at higher risk.
Check the product label for the NDC code 05446-0970-03. The recall includes specific batches sold between June 2021 and April 2022.
Look for the NDC code 05446-0970-03 on the product label to confirm if it is recalled.
The recall is due to manufacturing quality control issues, but no injuries have been reported. The product may not meet safety standards.
Check the product label for the NDC code 05446-0970-03 and the specific batch dates listed in the recall notice.
The recall does not specify a remedy, so contact Edge Pharma directly for guidance.
We’ve drafted a message you can send Edge Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0430-2022 — Edge Pharma Edge Pharma Hello, I own a Edge Pharma that is covered by recall D-0430-2022 from Edge Pharma. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
