Kenil Healthcare recalls Nature Mint Anticavity Fluoride Toothpaste due to CGMP deviations. This may affect safety standards. Check product details to see if you have the recalled batch.
CGMP Deviations
Kenil Healthcare is recalling Nature Mint Anticavity Fluoride Toothpaste with sodium monofluorophosphate 0.76% due to manufacturing quality control issues. This recall does not involve immediate safety risks but requires checking your product for the specific batch numbers listed.
CGMP deviations refer to failures in the manufacturing process that could affect product quality. This means the toothpaste might not meet the required safety and quality standards for use. However, the recall does not indicate an immediate risk of injury or harm.
Owners of Nature Mint Anticavity Fluoride Toothpaste with the specified batch 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 batch numbers: B0004 (exp 05/31/2026), B0060 (exp 07/31/2026), B0067/B0071/B0072 (exp 08/31/2026), or B0107/B0108 (exp 09/30/2026). The product is sold in 1.5 oz tubes with the manufacturer's address in India.
Look for the batch numbers and expiration dates listed on the tube label to determine if your product is recalled.
The recall is due to manufacturing quality control issues, but the product is not considered unsafe for immediate use. Check the batch numbers to see if it's part of the recall.
Check the tube label for batch numbers: B0004 (exp 05/31/2026), B0060 (exp 07/31/2026), B0067/B0071/B0072 (exp 08/31/2026), or B0107/B0108 (exp 09/30/2026).
No, the recall does not require stopping use. Check the batch numbers to see if your product is affected.
We’ve drafted a message you can send Kenil Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0439-2025 — Kenil Healthcare Kenil Healthcare Hello, I own a Kenil Healthcare that is covered by recall D-0439-2025 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.
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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.
