FDA alerts consumers of nationwide voluntary recall of EpiPen and EpiPen Jr

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Title: FDA alerts consumers of nationwide voluntary recall of EpiPen and EpiPen Jr

 
u s food and drug administration

News Release

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03/31/2017 06:34 PM EDT

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.

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