DTCClass 2
Analyzer, Pacemaker Generator Function
FDA adverse event reports and recall history for analyzer, pacemaker generator function (product code DTC), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 3,826
- Deaths
- 3
- Injuries
- 152
- Malfunctions
- 3,669
Reports per year
104
606
210
111
114
3417
2218
13919
18920
63521
21722
21023
1,06624
1,19425
4626
Source: FDA adverse event reports by year received, 2004–2026. 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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