April 2022 FDA Recall Rifampin by Mylan Pharmaceuticals Inc
D-0774-2022 - Failed Impurities/Degradation Specifications

This Class II drug recall was voluntarily initiated by Mylan Pharmaceuticals Inc on April 7, 2022 for the product Rifampin. The FDA reported the reason for recall as failed impurities/degradation specifications. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0774-2022

Reason for Recall
Failed Impurities/Degradation Specifications: High out of specification results obtained for related compound during stability testing.
Initiated
04-07-2022
Reported
04-27-2022
Quantity
33,893 vials

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Mylan Pharmaceuticals Inc
Nationwide in the USA
Rifampin for Injection, USP, 600 mg/vial, One Vial per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505 U.S.A., NDC 67457-445-60

Batch or Lot Expiration Information

Lot# : 7008990, exp. date Dec-2022; 7009025, exp. date Feb-2023; 7009085, 7009086, exp. date Apr-2023

Affected Packages Involved in this Recall