MYLAN PHARMACEUTICALS INC 2026-08-05 Health serious FDA
Health · FDA · Recall #FDA-D-0734-2026
Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per… Recall
Issued August 5, 2026 · MYLAN PHARMACEUTICALS INC
In August 2026, MYLAN PHARMACEUTICALS INC recalled the Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per…, a serious health recall reported by the FDA.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
Presence of precipitate
What you should do
- 1 Stop using Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact MYLAN PHARMACEUTICALS INC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- MYLAN PHARMACEUTICALS INC
- Category
- Health
- Recall date
- August 5, 2026
- Units affected
- Not reported
- Sold at
- USA Nationwide
- Recall number
- FDA-D-0734-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- MYLAN PHARMACEUTICALS INC has 2 recalls in our database.
- We're tracking 3,707 Health recalls in our database.
- This is the 487th Health recall we've logged in 2026.