Drug recall D-0734-2026
Product
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).
Reason for recall
Presence of precipitate
Lots and codes
Lot #: 3241653, Exp 4/30/2027
Recall details
- Recalling firm
- MYLAN PHARMACEUTICALS INC, Morgantown, WV
- Quantity
- 5688 vials
- Distribution
- USA Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 2, 2026
Related products
- Mycophenolate Mofetil – drug information
- NDC 67457-386 Mycophenolate Mofetil · Mycophenolate Mofetil 500 mg/20mL · Mylan Institutional LLC