US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 5, 2018 (9 years ago)

methylPREDNISolone Sodium Succinate for Injection, USP, 125 mg* per vial, Single-Dose…

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

Why it was recalled

Failed Impurities/Degradation Specifications: High out of specification results for an impurity.

What was recalled

methylPREDNISolone Sodium Succinate for Injection, USP, 125 mg* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-808-10.

Recalling firm
Sagent Pharmaceuticals Inc
NDC code
25021-808-10
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0587-2018

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 Methylprednisolone recalls

See all