US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 7, 2019 (7 years ago)

Rifampin for Injection, USP, 600 mg/vial, Rx only, Manufactured for: Mylan Institutional…

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

Why it was recalled

Failed Impurities/Degradation Specifications: discoloration due to elevated unknown impurity results which could decrease the effectiveness of the product.

What was recalled

Rifampin for Injection, USP, 600 mg/vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103; NDC 67457-445-60.

Recalling firm
Mylan Laboratories Limited (Sterile Products Division)
NDC code
67457-445-60
Origin
N/A, India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0139-2020

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.

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