United StatesMycophenolate Mofetil for Injection USP, 500 mg single‑dose vials (4 vials per carton) manufactured for Mylan Institutional LLC (Made in India), NDCs 67457-386-00 (vial) and 67457-386-81 (carton), Lot #3241653, exp. 4/30/2027, is being recalled nationwide in the U.S. The recall is due to the presence of precipitate.
What's being recalled
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).
Recalling firm: Mylan Pharmaceuticals Inc, Morgantown, WV, United States.
How to identify it
Lot #: 3241653, Exp 4/30/2027
The hazard
Presence of precipitate
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
USA Nationwide
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)