FDAFDA · Food and drugs·Recall number D-0734-2026
Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV, 26505 USA, Made in India, NDC 67457-386-00 (vial label) & NDC 67457-386-81 (carton label).
Published August 5, 2026 · Recall initiated: July 2, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of precipitate
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- MYCOPHENOLATE MOFETIL
- Manufacturer
- MYLAN PHARMACEUTICALS INC
- Distributor
- USA Nationwide
- Lot
- Lot #: 3241653, Exp 4/30/2027
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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