FDA Alert;Specific Units of the LIFEPAK® 15 Monitor/Defibrillator-Voluntary Recall

 MedWatch - The FDA Safety Information and Adverse Event Reporting Program

Stryker Launches Voluntary Field Action for Specific Units of the LIFEPAK® 15 Monitor/Defibrillator
A new MedWatch Safety Alert Recall LIFEPAK® 15 Monitor/Defibrillator by Stryker: Recall - Due to Lock Up (blank monitor display with LED lights on) after a Defibrillation Shock is Delivered was just added to the FDA Recalls web page.

You can read the complete recall at: https://www.fda.gov/Safety/Recalls/ucm630455.ht