DTDClass 2
Pacemaker Lead Adaptor
FDA adverse event reports and recall history for pacemaker lead adaptor (product code DTD), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 741
- Deaths
- 40
- Injuries
- 457
- Malfunctions
- 232
Reports per year
1912
3013
2114
4115
2016
1617
2918
3419
1920
2321
2522
2823
3524
3225
1526
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor pacemaker lead adaptor 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.