Device Lookup

For Assurity and Endurity Pacemaker Equipment Safety Notification

In October 2023, Abbott provided a Safety Notification informing clinicians of the potential for device malfunction due to a manufacturing issue which may affect a limited subset of 455 Assurity™ and Endurity™ pacemakers.

Physician Communication - Europe - English (PDF 134kb)

Visit our Product Advisories page for translated, country letters

This tool enables healthcare professionals to confirm if a specific device is subject to this safety notification.

Device Lookup Instructions

Please follow the steps below to determine if an Assurity or Endurity pacemaker is subject to this safety notification.

  1. Enter the device model and serial number below; both are required.
  2. If the device is subject to this notification, review the patient management recommendations in the safety notification.
  3. If the device is not subject to this notification, no further action related to this notification is needed.

If you are a patient and have questions about your device, please contact your treating physician.

Check a Device

Enter the four digit model number without the prefix (PM). Next, enter the entire serial number.  

Please enter a valid model and serial number. Enter the four digit model number without the prefix (PM). Next, enter the entire serial number. Please enter model number
Please enter a valid model and serial number. Enter the four digit model number without the prefix (PM). Next, enter the entire serial number. Please enter serial number

Please note, this device lookup tool is specific to the 2023 advisory. To look up whether the device is subject to a prior advisory, please refer to the respective Product Advisories lookup tools listed above.

MAT-2311632 v2.0