MedicineWatch US
Class III Recall

VistaPharm LLC

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
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
Classification
Class III
Status
Terminated
Lot
Lot #: M23400A, M23401A, M23402A, Exp Date. 04/30/2025; M23591A, M23592A, Exp Date. 06/30/2025.
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
VistaPharm LLC — Class III Recall | MedicineWatch US