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Vancomycin Hydrochloride for Injection Recall
Posted By Admin on January 08, 2018
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Vancomycin Hydrochloride for Injection, USP, 750 mg/vial

Hospira Inc. is voluntarily recalling one lot of Vancomycin Hydrochloride for Injection, USP, 750 mg/vial. This recall was classified as a Class I Recall on 12/27/2017 by the Food and Drug Administration (FDA).

The presence of particulate matter, confirmed as glass, was found within a single vial.

Please read the Hospira Inc. press release for more information.