Device Lookup

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 potentially susceptible to this issue which is caused by intermittent incomplete mixing of epoxy during manufacture that may potentially 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.

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.

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