PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: June 1, 2016 Initiated: April 27, 2016 #D-0868-2016

Product Description

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

Reason for Recall

Lack of Assurance of Sterility: Due to potential for leaking bags.

Details

Recalling Firm
Teva North America
Units Affected
546 bags
Distribution
Nationwide
Location
Horsham, PA

Frequently Asked Questions

What product was recalled?
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. Recalled by Teva North America. Units affected: 546 bags.
Why was this product recalled?
Lack of Assurance of Sterility: Due to potential for leaking bags.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 1, 2016. Severity: Moderate. Recall number: D-0868-2016.