VistaPharm, Inc.: Drug Recall
Recall #D-0376-2022 · 01/07/2022
Class II: Risk
Recall Details
- Recall Number
- D-0376-2022
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- VistaPharm, Inc.
- Status
- Terminated
- Date Initiated
- 01/07/2022
- Location
- Largo, FL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 18,456 bottles
Reason for Recall
Failed Stability Specifications
Product Description
Clobazam Oral Suspension 2.5 mg/mL, 120 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-058-04
Distribution Pattern
Nationwide within the United States including Puerto Rico
Other Recalls by VistaPharm, Inc.
- Class II: Risk 09/30/2022
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.