On March 15, 2021, Abbott began informing 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.
Physician Communication – Assurity and Endurity Pacemaker 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.
MAT-2103930 v1.0
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Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company.
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The following pages are intended for medical professionals and provide information on the proper use of products (medical devices, etc.) of Abbott Medical Japan GK.
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