Drug recall D-0093-2024
Product
Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.
Reason for recall
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
Lots and codes
Lot #: M23400A, M23401A, M23402A, Exp Date. 04/30/2025; M23591A, M23592A, Exp Date. 06/30/2025.
Recall details
- Recalling firm
- VistaPharm LLC, Largo, FL
- Quantity
- 11,633 bottles
- Distribution
- Nationwide and Saudi Arabia
- Type
- Voluntary: Firm initiated
- Recall initiated
- October 26, 2023
- Terminated
- March 21, 2025
Related products
- Mycophenolate Mofetil – drug information
- NDC 66689-307 Mycophenolate Mofetil · Mycophenolate Mofetil 200 mg/mL · VistaPharm, LLC