Teva North America recalls Linezolid Injection 600 mg/300 mL Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 1
Recalled September 14, 2016 · FDA recall D-1495-2016 · Teva North America
Hazard
CGMP Deviations · FDA Class II
Units
92,480 containers
Sold at
Nationwide and Puerto Rico
Description
CGMP Deviations
Product
Linezolid Injection 600 mg/300 mL Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-9060-31- (Single Use Container), NDC# 0703-9060-33 (Box of 10 Singe Use Containers)
Manufacturer(s)
Teva North America
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →