This tool enables healthcare professionals to confirm if a specific device is subject to this safety notification.
On October 5, 2021 and March 15, 2021 Abbott informed customers of an issue which may affect a subset of Assurity™ and Endurity™ pacemakers that include models: PM1152, PM1160, PM1172, PM1240, PM1272, PM2152, PM2160, PM2172, PM2240, PM2260, and PM2272. Abbott has identified a subset of devices that are potentially susceptible to this issue which is caused by intermittent incomplete mixing of epoxy during manufacture and may allow moisture ingress into the pulse generator header.
This tool enables healthcare professionals to confirm if a specific device is subject to this safety notification.
Please follow the steps below to determine if an Assurity or Endurity pacemaker is subject to this global safety notification.
If you are a patient and have questions about your device, please contact your treating physician.
Enter the four digit model number without the prefix (PM). Next, enter the entire serial number.
Please note that a separate device lookup tool is linked above for the July 2022 Zenex, Assurity, and Endurity pacemaker laser adhesion advisory.
MAT-2103930 v3.0
You are about to enter an Abbott country- or region-specific website.
Please be aware that the website you have requested is intended for the residents of a particular country or countries, as noted on that site. As a result, the site may contain information on pharmaceuticals, medical devices and other products or uses of those products that are not approved in other countries or regions
Do you wish to continue and enter this website?
MAT-2305078 v1.0