FDAFDA · Food and drugs·Recall number D-1234-2015
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
Published July 22, 2015 · Recall initiated: June 4, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications; out-of-specification for color, impurity, and degradation
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- RIFAMPIN
- Manufacturer
- Fresenius Kabi USA, LLC
- Distributor
- Nationwide,Hawaii, and Puerto Rico
- UPC
- 0363323351205
- Lot
- Lot #: 6109469, 6109470, Exp 10/2016
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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