FDA recall D-0455-2022

Dental Alliance Holdings LLC · Class III · drug

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 Oral BioTech Albany, Oregon 97321 and three bottles of CariFree CTx3 Rinse, Mint Anticavity Rinse, 16 fl oz. bottle.

Reason for recall

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

Distribution

Distributed nationwide with the United States

Key facts

Status
Terminated
Initiation date
2021-12-03
Report date
2022-02-02
Termination date
2022-08-11
Voluntary/Mandated
Voluntary: Firm initiated
Location
Albany, OR, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0455-2022