Telectronics Pacing Systems
FDA adverse event reports naming Telectronics Pacing Systems as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: TELECTRONICS PACING SYSTEMS.
- Total reports
- 3,057
- Deaths
- 25
- Injuries
- 1,730
- Malfunctions
- 1,279
Reports per year
2706
4607
2808
2009
610
1511
512
7413
1314
815
716
1317
218
122
223
Source: FDA adverse event reports by year received, 2006–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Permanent Pacemaker ElectrodeDTB2,409
- Implantable Pacemaker Pulse-GeneratorDXY615
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP24
- Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)JOQ4
- Pacemaker Lead AdaptorDTD2
- Implantable Cardioverter Defibrillator (Non-Crt)LWS2
- Product code 1
- Pulse-Generator, Pacemaker, ExternalDTE1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Telectronics Pacing Systems automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.