FDAFDA · Food and drugs·Recall number D-0093-2024
Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.
Published November 15, 2023 · Recall initiated: October 26, 2023
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- MYCOPHENOLATE MOFETIL
- Manufacturer
- VistaPharm LLC
- Distributor
- Nationwide and Saudi Arabia
- Lot
- Lot #: M23400A, M23401A, M23402A, Exp Date. 04/30/2025; M23591A, M23592A, Exp Date. 06/30/2025.
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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