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# Abbott Recall of 2 Pacemaker Models is Class 1
- URL: https://www.fdaweb.com/abbott-recall-of-2-pacemaker-models-is-class-1/
- Published: 2021-05-13T12:00:00.000Z
- Updated: 2026-09-14T16:58:45.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149318

FDA says an Abbott (St. Jude Medical) 3/15 recall of a subset of Assurity and Endurity pacemakers is Class 1\. An agency [notice](https://www.fda.gov/medical-devices/medical-device-recalls/abbott-formally-known-st-jude-medical-recalls-assuritytm-and-enduritytm-pacemakers-potential?ref=fdaweb.com) says Assurity and Endurity are implantable bradycardia pacemakers. The notice says the company recalled a subset of the pacemakers distributed from 4/2015 to 2/2019 because a small number of devices from that time frame have experienced problems when moisture can enter the device, causing an electrical short.

FDA says there have been 135 complaints, 135 injuries, and no deaths reported for this issue.