Kenil Healthcare recalls specific lots of Maximum Security Anticavity Gel Toothpaste (Sodium Fluoride 0.22%) due to CGMP deviations. Consumers should check product details and contact the company for instructions.
CGMP Deviations
Kenil Healthcare is recalling certain lots of Maximum Security Anticavity Gel Toothpaste because of manufacturing deviations. This recall affects toothpaste sold in India with specific lot numbers and expiration dates.
The recall is due to CGMP (Current Good Manufacturing Practice) deviations, which means the toothpaste may not meet safety and quality standards. However, the specific hazard is not detailed in the recall notice.
Owners of the recalled toothpaste, particularly those who purchased it in India with the listed lot numbers and expiration dates. People using this toothpaste regularly are most at risk.
Check the product label for the lot numbers B0008, B0009, B0017 (expiring 05/31/2026), B0042, B0043, B0044 (expiring 06/30/2026), B0049, B0050, B0051, B0054, B0058, B0059 (expiring 07/31/2026), or B0061, B0062, B0063, B0064, B0065, B0068, B0069 (expiring 08/31/2026).
Look for the lot numbers and expiration dates listed in the recall notice to confirm if your toothpaste is affected.
The recall is due to CGMP deviations, which means the toothpaste may not meet safety and quality standards. The specific hazard is not detailed in the notice.
Check the product label for the lot numbers B0008, B0009, B0017 (expiring 05/31/2026), B0042, B0043, B0044 (expiring 06/30/2026), B0049, B0050, B0051, B0054, B0058, B0059 (expiring 07/31/2026), or B0061, B0062, B0063, B0064, B0065, B0068, B0069 (expiring 08/31/2026).
The recall notice does not specify a remedy, so contact Kenil Healthcare directly for instructions.
We’ve drafted a message you can send Kenil Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0432-2025 — Kenil Healthcare Kenil Healthcare Hello, I own a Kenil Healthcare that is covered by recall D-0432-2025 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.
