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 corpus and the live FDA recall database.
- Total reports
- 228,094
- Deaths
- 5,055
- Injuries
- 128,126
- Malfunctions
- 94,775
Reports per year
5,88812
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
13,70926
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.
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