FDARecall 99750Medicines
What to do
The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.
Read the official notice on accessdata.fda.gov (opens in a new tab)
Hazard
Why it was recalled
Failed Dissolution Specifications
FDA classification: Class II. Use may cause temporary or medically reversible health consequences, or the chance of serious consequences is remote. Status: Ongoing.
Is it yours? Products and codes
Carton label: Mycophenolate Mofetil for injection, USP, 500 mg/vial, Sterile, 4 Single Dose Vials, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505, Made in India, NDC 67457-386-81. Vial Label: Mycophenolate Mofetil for injection, USP, 500 mg/vial, Sterile, Single Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505, Made in India, NDC 67457-386-00.
- Lot or code
- Lot: 3242616, Exp. April 2027; 8220216, Exp. Nov 2027
- FDA recall number
- D-0830-2026
- Quantity
- 11,336 units
Distribution (FDA): U.S. Nationwide
About this record
- Issued by
- U.S. Food and Drug Administration
- Firm
- Mylan Pharmaceuticals Inc (other notices of this firm)
- Title
- Composed by Recalls Watch from fields of the record; FDA records have no title.