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Effective February 3, 2021, 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.

Please fill out the form below for more information.