DTDClass 2
Pacemaker Lead Adaptor
FDA adverse event reports and recall history for pacemaker lead adaptor (product code DTD), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 737
- Deaths
- 40
- Injuries
- 456
- Malfunctions
- 229
Reports per year
1912
3013
2114
4115
2016
1617
2918
3419
1920
2321
2522
2823
3524
3225
1126
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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