Ecometics, Inc.: Drug Recall
Recall #D-0451-2023 · 02/24/2023
Class II: Risk
Recall Details
- Recall Number
- D-0451-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Ecometics, Inc.
- Status
- Terminated
- Date Initiated
- 02/24/2023
- Location
- Norwalk, CT, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 34,320 bottles
Reason for Recall
CGMP DEVIATIONS
Product Description
Activator Concentrate (sodium fluoride 0.96% in Activator) 1 fl. Oz, liquid oral rinse plastic bottles, Manufactured for: All USA Direct LLC, Broadview, IL 60155
Distribution Pattern
Nationwide within the United States
Other Recalls by Ecometics, Inc.
- Class II: Risk 08/09/2023
- Class II: Risk 08/09/2023
- Class II: Risk 08/09/2023
- Class II: Risk 08/09/2023
- Class II: Risk 08/09/2023
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.