Edge Pharma recalls 30g Raspberry Marshmallow dental gel with CGMP deviations. Products sold from July 2021 to April 2022 may pose quality risks. Consumers should contact Edge Pharma for details.
CGMP Deviations
Edge Pharma is recalling a specific dental gel product due to manufacturing quality issues. This recall is for products sold between July 2021 and April 2022 that may have quality problems. The recall does not mention specific safety risks like injury or illness.
The recall mentions CGMP deviations, which are manufacturing quality issues. However, the record does not specify what these deviations mean for safety or health. The hazard description is too vague to determine if there's a real risk.
People who own or use the recalled dental gel product are affected. Those who purchased the product between July 2021 and April 2022 are most at risk.
Check for the product name: Profound Dental Gel, 10%/10%/4% Raspberry Marshmallow, 30 grams per jar. Products were sold from July 2021 to April 2022 with specific NDC numbers.
Look for the product name and NDC numbers listed in the recall notice to confirm if your item is affected.
The recall mentions CGMP deviations but does not specify safety risks. The official notice does not state if the product is safe or unsafe.
The recall covers products sold from July 2021 to April 2022.
Contact Edge Pharma at 856 Hercules Dr. Colchester, VT 05446 for details about the recall.
We’ve drafted a message you can send Edge Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0439-2022 — Edge Pharma Edge Pharma Hello, I own a Edge Pharma that is covered by recall D-0439-2022 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.