Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Rifampin for Injection Recalled by Mylan Pharmaceuticals Inc Due to Failed Impurities/Degradation Specifications: High out of specification results...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mylan Pharmaceuticals Inc directly.
Affected Products
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
Quantity: 33,893 vials
Why Was This Recalled?
Failed Impurities/Degradation Specifications: High out of specification results obtained for related compound during stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mylan Pharmaceuticals Inc
Mylan Pharmaceuticals Inc has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report