Dental Alliance recalls CTx21 Kit (3 tubes of CariFree CTx4 Gel 5000) due to less sodium fluoride than labeled. This subpotent drug may not provide adequate cavity prevention. Contact for return instructions.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Dental Alliance is recalling CTx21 kits because they contain less sodium fluoride than labeled. This means the product may not effectively prevent cavities as intended. Consumers should stop using the product and contact the company for a replacement.
The product contains less sodium fluoride than stated on the label. This subpotent drug may not provide the intended cavity prevention benefits. The risk is low as it does not cause immediate harm but affects the product's effectiveness.
People who own the CTx21 kit (three tubes of CariFree CTx4 Gel 5000) purchased between 2021 and 2022 are affected. Those using the product for cavity prevention are most at risk.
Check for the CTx21 kit with three tubes of CariFree CTx4 Gel 5000. The kit was manufactured with lot numbers 272109 or 272110 and expires June 2022.
Immediately stop using the recalled CTx21 kit as it contains less sodium fluoride than labeled.
The product may not provide adequate cavity prevention due to less sodium fluoride than labeled, but it is not harmful.
Check for the CTx21 kit with three tubes of CariFree CTx4 Gel 5000, manufactured with lot numbers 272109 or 272110 and expiring June 2022.
Contact Dental Alliance Holdings LLC for a replacement or return instructions.
We’ve drafted a message you can send Dental Alliance Holdings LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0455-2022 — Dental Alliance Holdings LLC Dental Alliance Holdings LLC Hello, I own a Dental Alliance Holdings LLC that is covered by recall D-0455-2022 from Dental Alliance Holdings LLC. 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.
