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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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