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.
Class II · Ongoing
Presence of precipitate
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Affected lots / codes — check yours against thisLot #: 3241653, Exp 4/30/2027
- Recalling firm
- MYLAN PHARMACEUTICALS INC, Morgantown, WV
- Classification
- Class II (temporary or reversible harm possible)
- Status
- Ongoing
- Quantity
- 5688 vials
- Distribution
- USA Nationwide
- Recall initiated
- July 2, 2026
- Classified
- August 4, 2026
- Initiation
- Voluntary: Firm initiated
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Official source. This record is published by the U.S. FDA through the openFDA
enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0734-2026%22
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0734-2026%22
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Important. Recalls target specific lots and codes — compare the affected lots
above against your own product. This page reproduces public FDA data for readability;
EveryRecall is independent and not affiliated with the FDA.
Check this brand across all 8 databases →