Ohio State Navbar

FDA News Release: FDA alerts consumers of nationwide voluntary recall of EpiPen and EpiPen Jr


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.

Consumers should contact Mylan at 800-796-9526 or customer.service@mylan.com with any questions.

Click here for full FDA news release.