US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 3, 2021 (5 years ago)

CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 GEl 5000 gel tubes. 1.1% Neutral…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.

What was recalled

CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 GEl 5000 gel tubes. 1.1% Neutral Sodium Fluoride Mint, 2 oz (57 g) Rx only NDC: 61578-205-01 Manufactured by Oral BioTech Albany, Oregon 97321.

Recalling firm
Dental Alliance Holdings LLC
Origin
OR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0459-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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