NVNClass 3
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA adverse event reports and recall history for drug eluting permanent right ventricular (rv) or right atrial (ra) pacemaker electrodes (product code NVN), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 226,220
- Deaths
- 5,038
- Injuries
- 127,063
- Malfunctions
- 93,983
Reports per year
5,88912
7,65313
9,88614
10,13715
9,39316
11,61317
11,51918
16,87319
16,52920
17,75721
18,20022
24,99123
22,01424
23,65625
11,83426
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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