Drug recall D-1234-2015
Product
Rifampin for Injection, USP 600mg/vial in a 20mL vial, Rx only, Manufactured for Fresenius Kabi LLC 3 Corporate Drive, Lake Zurich, IL, 60047, by Fresenius Kabi LLC, 2020 N Ruby Street, Melrose Park, IL 60160. NDC 63323-351-20
Reason for recall
Failed Impurities/Degradation Specifications; out-of-specification for color, impurity, and degradation
Lots and codes
Lot #: 6109469, 6109470, Exp 10/2016
Recall details
- Recalling firm
- Fresenius Kabi USA, LLC, Lake Zurich, IL
- Quantity
- 7,593 vials
- Distribution
- Nationwide,Hawaii, and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- June 4, 2015
- Terminated
- May 19, 2016
Related products
- Rifampin – drug information
- NDC 63323-351 Rifampin · Rifampin 600 mg/1 · Fresenius Kabi USA, LLC