Kenil Healthcare recalls Maximum Security Anticavity Gel Toothpaste with CGMP deviations. Products made in India, distributed by Bob Barker Co. Inc. in NC. Affected lots expire May 2026 through August 2026.
CGMP Deviations
Kenil Healthcare is recalling Maximum Security Anticavity Gel Toothpaste due to CGMP deviations. This means the toothpaste may not meet quality standards, though the specific risk isn't detailed in the recall notice.
CGMP deviations refer to failures in manufacturing quality control processes. This could mean the toothpaste doesn't meet safety or quality standards, but the recall doesn't specify the exact risk.
People who own or use the recalled Maximum Security Anticavity Gel Toothpaste. Those with the specific lots listed (B0009, B0017, etc.) are most at risk.
Check the product label for the lot numbers: B0009, B0017, B0018, B0019, B0036, B0037, B0038, B0049, or B0063. Products were made in India and distributed by Bob Barker Co. Inc. in North Carolina.
Look for the lot numbers listed: B0009, B0017, B0018, B0019, B0036, B0037, B0038, B0049, or B0063 on the tube.
The recall is due to CGMP deviations, which means the toothpaste may not meet quality standards, but the specific risk isn't detailed in the notice.
Check the product label for the lot numbers listed. If you have the affected lots, you should stop using it and contact the manufacturer for further instructions.
Check the label for lot numbers: B0009, B0017, B0018, B0019, B0036, B0037, B0038, B0049, or B0063. Products were made in India and distributed by Bob Barker Co. Inc. in North Carolina.
We’ve drafted a message you can send Kenil Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0431-2025 — Kenil Healthcare Kenil Healthcare Hello, I own a Kenil Healthcare that is covered by recall D-0431-2025 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.
