Effective February 3, 2022, accessories and service for non-FDA-approved AEDs and professional defibrillators will no longer be supported by the manufacturer. This will impact ZOLL® M Series® and E Series® monitor/defibrillators users as well as users of any other non-FDA-approved device.
To learn more, including how to determine whether your devices are FDA-approved and what steps you should take if they are not, please complete this form. We will contact you with more information
A message from Elijah White, President of ZOLL Resuscitation
