Dental Alliance Holdings recalls CariFree sample boxes with less sodium fluoride than labeled, risking inadequate cavity prevention. Consumers should check product details and contact the company for guidance.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Dental Alliance Holdings is recalling CariFree sample boxes that contain less sodium fluoride than listed on the label. This could lead to inadequate cavity prevention if used as intended.
The product contains less sodium fluoride than stated on the label, which may result in insufficient cavity prevention. This is a subpotent drug issue, meaning the active ingredient is less concentrated than advertised.
People who own or use CariFree sample boxes with the specific lot numbers mentioned in the recall. Those most at risk are individuals relying on the product for dental health maintenance.
Check for CariFree sample boxes with lot numbers 492106 or 492107, manufactured by Oral BioTech in Albany, Oregon, and expiring June 2022. The product contains one tube of CariFree CTx4 Gel 5000, 1.1% Neutral Sodium Fluoride Mint, 2 oz (57 g).
Look for lot numbers 492106 or 492107 on the CariFree sample boxes, which were manufactured by Oral BioTech in Albany, Oregon and expire June 2022.
The product contains less sodium fluoride than listed on the label, which may result in inadequate cavity prevention.
Check for CariFree sample boxes with lot numbers 492106 or 492107, manufactured by Oral BioTech in Albany, Oregon, and expiring June 2022.
The recall does not specify a remedy, so contact Dental Alliance Holdings for guidance.
We’ve drafted a message you can send Dental Alliance Holdings to request your refund or repair — edit it as you like.
Subject: Recall D-0458-2022 — Dental Alliance Holdings Dental Alliance Holdings Hello, I own a Dental Alliance Holdings that is covered by recall D-0458-2022 from Dental Alliance Holdings. 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.
