Recalling firm
VistaPharm LLC
Product type
Drug
Status
Terminated
Report date
2023-11-15
Distribution
Nationwide and Saudi Arabia
Firm state
FL
Product quantity
11,633 bottles
Initiated by
Voluntary: Firm initiated
Reason for recall
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
Product description
Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.
Code / lot info
Lot #: M23400A, M23401A, M23402A, Exp Date. 04/30/2025; M23591A, M23592A, Exp Date. 06/30/2025.
Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.