US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 5, 2020 (6 years ago)

Aloprim (allopurinol sodium) for Injection, 500 mg Single-Dose Vial, Rx only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Discoloration: Out-of-specification results for appearance obtained during routine stability testing at the end of shelf-life for the parameters Appearance and Color of Solution.

What was recalled

Aloprim (allopurinol sodium) for Injection, 500 mg Single-Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 USA. NDC: 67457-187-50

Recalling firm
Mylan Institutional LLC
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1271-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Allopurinol recalls

See all