FDA alerts consumers of nationwide voluntary recall of EpiPen and EpiPen Jr - FDA Press Releases

The U.S. Food and Drug Administration is alerting consumers to Meridian Medical Technologies’ voluntary recall of 13 lots of Mylan’s EpiPen and EpiPen Jr (epinephrine injection) Auto-Injector products used for emergency treatment of severe allergic reactions. This recall is due to the potential that these devices may contain a defective part that may result in the devices’ failure to activate. The recalled product was manufactured by Meridian Medical Technologies and distributed by Mylan Specialty.

from Food and Drug Administration--Press Releases http://ift.tt/2oqP2F7
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