Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class III · Low risk Terminated Initiated Dec 3, 2021 (5 years ago)

CTx26 Kit

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.

Cause type: Wrong potency / content

Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.

What was recalled

CTx26 Kit, contains three tubes of CariFree CTx4 Gel 5000, 1.1% Neutral Sodium Fluoride Mint, 2 oz (57 g) Rx only NDC: 61578-205-01 Manufactured by Oral BioTech Albany, Oregon 97321 and two bottles of CariFree CTx3 Rinse, Mint Anticavity Rinse, 16 fl oz. bottle an two boxes of 4fl.oz. Carifree CTx4 Treatment Rinse.

Affected NDC 61578-0205-01

Compare with the code on your package — it is the most precise check available.

Drug: Fluoride

Recalling firm
Dental Alliance Holdings LLC
Origin
OR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0456-2022 · FDA notice

Low risk, still worth a check. Class III means the product is unlikely to cause harm but breaks an FDA rule (often labeling). If your lot matches, your pharmacy will normally swap it; there is no need for alarm. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Fluoride recalls

See all
Class III · Low risk

Sensodyne PRONAMEL

Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is labelled Cool Mint/Whitening. The toothpaste inside the tube is Fresh Mint as indicated on the outer carton

Ongoing Labeling / mix-up Haleon US Holdings LLC D-0592-2025
Class II · Moderate risk

Nature Mint

CGMP Deviations

Terminated cGMP deviation Kenil Healthcare Private Limited NDC 53247-131-05 D-0440-2025
Class II · Moderate risk

Nature Mint

CGMP Deviations

Terminated cGMP deviation Kenil Healthcare Private Limited NDC 53247-131-07 D-0437-2025

Other recalls by Dental Alliance Holdings LLC

All 2021 recalls
Class III · Low risk

CTx36 Kit

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

Terminated Wrong potency / content Dental Alliance Holdings LLC D-0457-2022
Class III · Low risk

CTx21 Kit

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

Terminated Wrong potency / content Dental Alliance Holdings LLC D-0455-2022