Den-Mat Holdings recalls hydrogen peroxide oral rinse products due to potential failure to meet labeled specifications. Consumers should check product details and contact the manufacturer for guidance.
CGMP Deviations: products may not conform to the labeled specifications.
Den-Mat Holdings is recalling hydrogen peroxide oral rinse products that may not meet their labeled specifications. This could affect product safety and effectiveness, though no injuries have been reported.
The recall is due to the products not meeting the labeled specifications as per current Good Manufacturing Practices (CGMP). This means the rinse might not work as intended for reducing bacteria, but it does not indicate a risk of injury or serious harm.
People who own or use Den-Mat hydrogen peroxide oral rinse products with the listed lot numbers and expiration dates are affected. Those with the product in their homes or on their person are most at risk.
Check for the product name 'Hydrogen Peroxide Oral Rinse, Significantly Reduces Bacteria, Fresh Mint Flavor, Alcohol Free' with the listed lot numbers and expiration dates on the bottle. The NDC codes are 59883-202-16, 59883-202-64, and 59883-202-28.
Look for the product name, lot numbers, and expiration dates listed in the recall notice to confirm if your product is affected.
The recall states the products may not meet labeled specifications, but no injuries have been reported. Use with caution as effectiveness might be reduced.
Check the lot numbers and expiration dates on the bottle, which are listed in the recall notice for affected products.
The recall does not specify a remedy, so contact Den-Mat Holdings for further guidance.
We’ve drafted a message you can send Den-Mat to request your refund or repair — edit it as you like.
Subject: Recall D-0287-2024 — Den-Mat Den-Mat Hello, I own a Den-Mat that is covered by recall D-0287-2024 from Den-Mat. 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.
