Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
RIFAMPIN FOR INJECTION USP Recalled by Akorn, Inc. Due to Failed Impurity/Degradation Specifications: Out of Specifications result obtained...
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 Akorn, Inc. directly.
Affected Products
RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.
Quantity: 6861 Vials
Why Was This Recalled?
Failed Impurity/Degradation Specifications: Out of Specifications result obtained for a known impurity.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Akorn, Inc.
Akorn, Inc. has 176 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report