EpiPen Voluntary Recall Expanded to US

Mylan Announces Nationwide Epi Pen Recall Over Potential Defect
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03 April, 2017

This recall is being conducted following two confirmed worldwide reports of the device failing to activate. The devices, manufactured by Meridian Medical Technologies, were made between December 2015 and July 2016. The recalled devices may contain a defective part that could cause the pens to fail to activate.

EpiPen (0.3 mg epinephrine) auto-injector lot 5GU763, expiry date May 2017.

Mylan said in a release that the EpiPens that are recalled will be replaced at no cost.

"What they're asking consumers to do is to check to see if their EpiPens are in these lots, and if so, to send them back so they can send replacements", Childs said. (0.15 mg) are sold as 2 Pak Auto-Injectors.

The defect makes it hard for the EpiPen to work during an emergency and could have significant health consequences for someone who is experiencing an allergic reaction.

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For more information about the recall, visit the Health Canada website. The St.Louis, Missouri-based company initially did not include the United States in the recall, but later added them to the list. No device failures have been reported in the United States.

The U.S. recall follows an global recall of roughly 81,000 EpiPens in Australia, New Zealand, Europe and Japan in March.

Mylan is already suffering from bad PR after the company introduced a 600 percent price hike for the life saving device a year ago, an increase the CEO argued was "fair".

"We are asking patients to keep their existing product until their replacement product can be secured", the company said.


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