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Device Lookup

For Assurity and Endurity Pacemaker Equipment Safety Notification

Product Advisories

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.

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 that a separate device lookup tool is linked above for the March/October 2021 Assurity and Endurity advisory and the July 2022 Zenex, Assurity, and Endurity advisory.

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Information contained herein for distribution outside the U.S. only.

CAUTION: These products are intended for use by or under the direction of a physician. Prior to use, reference the Instructions for Use, inside the product carton (when available) or online for more detailed information on Indications, Contraindications, Warnings, Precautions and Adverse Events.

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