Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
CTx36 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug: Product contains less Sodium Fluoride than...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Dental Alliance Holdings LLC directly.
Affected Products
CTx36 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 six boxes of 4fl.oz. Carifree CTx4 Treatment Rinse.
Quantity: 90 single tubes of 352110 and 315 single tubes of 352111
Why Was This Recalled?
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Dental Alliance Holdings LLC
Dental Alliance Holdings LLC has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report