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Class II · ModerateActive recall

Mycophenolate Mofetil

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: 3241653, Exp 4/30/2027
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of precipitate

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byMade in India foreign manufacturer
Brand nameMYCOPHENOLATE MOFETIL
Generic nameMYCOPHENOLATE MOFETIL
Active ingredient(s)MYCOPHENOLATE MOFETIL
Distributed by / forMylan Institutional LLC, Morgantown, WV, 26505 USA, Made in India
NDC67457-386-00
Show the full FDA record
Full product labelMycophenolate 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 firmMYLAN PHARMACEUTICALS INC
DistributionUSA Nationwide
Quantity5688 vials
Recall initiated2026-07-02
Report date2026-08-05
Recall completed—
Recall numberD-0734-2026
ClassificationClass II
FDA statusOngoing
Origin on fileMorgantown WV United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.