CTx21 Kit recall: Subpotent
CTx21 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…
Why was CTx21 Kit recalled?
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 272109, 272110 Exp. Date 06/22; (contains recalled CariFree CTx4 5000 gel tube lot 142017)
- Product
- CTx21 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…
- Recalling firm
- Dental Alliance Holdings LLC
- Quantity
- 180 single tube of lot 272109 and 180 single tube count of lot 272110
- Distribution
- Distributed nationwide with the United States
- Recall date
- February 2, 2022
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)