Meridian Medical Technologies is in the midst of a voluntary recall of 13 lots of Mylan’s EpiPen and EpiPen Jr (epinephrine injection) auto-injector products used for the emergency treatment of severe allergic reactions, the FDA warned.
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 products were manufactured by Meridian Medical Technologies and distributed by Mylan Specialty.