Kenil Healthcare is recalling Nature Mint Anticavity Fluoride Toothpaste due to CGMP deviations. This affects specific lots and expiration dates. Consumers should check their product details and contact the manufacturer for instructions.
CGMP Deviations
Kenil Healthcare is recalling Nature Mint Anticavity Fluoride Toothpaste with sodium monofluorophosphate 0.76% due to manufacturing quality control issues. This recall affects specific lots and expiration dates, but the product is not expected to cause injury if used properly.
CGMP deviations refer to manufacturing quality control issues that could affect product safety and effectiveness. This means the toothpaste may not meet the required standards for quality and safety, but it does not pose an immediate risk of injury or illness.
Owners of Nature Mint Anticavity Fluoride Toothpaste with specific lot numbers and expiration dates are affected. Children and individuals with sensitive teeth may be at slightly higher risk due to the fluoride content.
Check the product label for the lot numbers B0027, B0031 (expiring 06/30/2026) or B0032 (expiring 07/31/2026). The product was distributed by Bob Barker Co. Inc. in Fuquay-Varina, NC.
Look for the lot numbers B0027, B0031 (expiring 06/30/2026) or B0032 (expiring 07/31/2026) on the toothpaste tube.
The recall is due to manufacturing quality control issues, but the product is not expected to cause injury if used properly. Consumers should check their product details and contact the manufacturer if unsure.
Check the product label for the lot numbers B0027, B0031 (expiring 06/30/2026) or B0032 (expiring 07/31/2026). If you have the affected product, contact Kenil Healthcare for instructions.
The recall record does not specify a replacement option. Contact Kenil Healthcare directly for further assistance.
We’ve drafted a message you can send Kenil Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0435-2025 — Kenil Healthcare Kenil Healthcare Hello, I own a Kenil Healthcare that is covered by recall D-0435-2025 from Kenil Healthcare. 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.
