Teva North America recalls Linezolid Injection, 600 mg/300 mL Single use container bags (NDC 0703-9060-31), packaged in 10 x 300 mL Single Use Cont
Recalled June 1, 2016 · FDA recall D-0868-2016 · Teva North America
Hazard
Lack of Assurance of Sterility: Due to potential for leaking bags. · FDA Class II
Units
546 bags
Sold at
Nationwide
Description
Lack of Assurance of Sterility: Due to potential for leaking bags.
Product
Linezolid Injection, 600 mg/300 mL Single use container bags (NDC 0703-9060-31), packaged in 10 x 300 mL Single Use Container bags per Box Pack (NDC 0703-9060-33), Rx only, Manufactured In Hungary By: Teva Pharmaceutical Works Ltd., Hungary, H-2100 Godollo, Tancsics M. ut 82 Hungary; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454
Manufacturer(s)
Teva North America
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →