RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.
Reported: November 25, 2015 Initiated: August 20, 2015 #D-0231-2016
Product Description
RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.
Reason for Recall
Failed Impurity/Degradation Specifications: Out of Specifications result obtained for a known impurity.
Details
- Recalling Firm
- Akorn, Inc.
- Units Affected
- 6861 Vials
- Distribution
- US: Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.. Recalled by Akorn, Inc.. Units affected: 6861 Vials.
Why was this product recalled? ▼
Failed Impurity/Degradation Specifications: Out of Specifications result obtained for a known impurity.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 25, 2015. Severity: Low. Recall number: D-0231-2016.
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