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Recall of Linezolid Injection 600mg/300mL flexible bags
Posted By Admin on February 26, 2018
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On December 20, 2017, AuroMedics Pharma LLC initiated a voluntary recall of one lot of Linezolid Injection. The product was distributed May 15, 2017 through August 14, 2017, to wholesalers/hospitals nationwide in the United States. This recall was classified as a Class I Recall on February 8, 2018 by the Food and Drug Administration (FDA).

Product from this lot was found to contain white particulate matter that has been identified as mold.

For more information, please contact Aurobindo Customer Service weekdays 9 a.m. to 5 p.m., Eastern Standard Time at 1-866-850-2876, option 1 (TTY 711).