Arcadia Posted April 2, 2017 Share Posted April 2, 2017 "The U.S. Food and Drug Administration is alerting consumers to Meridian Medical Technologies’ voluntary recalldisclaimer icon 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. While the number of reported failures is small, EpiPen products that potentially contain a defective part are being recalled because of the potential for life-threatening risk if a severe allergic reaction goes untreated. Consumers should keep and use their current EpiPens if needed until they get a replacement. Consumers should contact Mylan at 800-796-9526 or customer.service@mylan.com with any questions." Lot numbers in link https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm550170.htm 1 Quote Link to comment Share on other sites More sharing options...
Guest Posted April 2, 2017 Share Posted April 2, 2017 Thanks for the PSA - off to go compare lot numbers as soon as I'm home! Quote Link to comment Share on other sites More sharing options...
Anne in CA Posted April 2, 2017 Share Posted April 2, 2017 Just when Epi Pen stuff couldn't get any worse. 1 Quote Link to comment Share on other sites More sharing options...
momacacia Posted April 2, 2017 Share Posted April 2, 2017 Karma. 2 Quote Link to comment Share on other sites More sharing options...
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