MYLAN PHARMACEUTICALS INC recalls Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: M
Recalled August 5, 2026 · FDA recall D-0734-2026 · MYLAN PHARMACEUTICALS
Hazard
Presence of precipitate · FDA Class II
Units
5688 vials
Sold at
USA Nationwide
Description
Presence of precipitate
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).
Manufacturer(s)
MYLAN PHARMACEUTICALS INC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →