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).
Presence of precipitate
| Recalling firm | MYLAN PHARMACEUTICALS INC |
|---|---|
| Reason | Presence of precipitate |
| Risk class | Class II (Class II · moderate) |
| Status | Ongoing |
| Report date | Aug 5, 2026 |
| Initiated | Jul 2, 2026 |
| Region | WV, United States |
| Distribution | USA Nationwide |
| Quantity | 5688 vials |
| Code/Lot | Lot #: 3241653, Exp 4/30/2027 |
| Type | Voluntary: Firm initiated |
| Recall number | D-0734-2026 |
Official source
U.S. FDA — Recalls, Market Withdrawals & Safety Alerts fda.gov ↗You can re-verify each item on the official FDA site using its recall number. (Recall number: D-0734-2026)
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