Recall RadarMycophenolate 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…
Presence of precipitate
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- MYLAN PHARMACEUTICALS INC — Morgantown, WV
- Severity
- Class II — moderate
- Reported
- August 5, 2026
- Quantity
- 5688 vials
- Recall number
- D-0734-2026
- Status
- Ongoing
- Source
- FDA
Where it went
USA Nationwide
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