OJXClass 3
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA adverse event reports and recall history for drug eluting permanent left ventricular (lv) pacemaker electrode (product code OJX), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 52,206
- Deaths
- 1,856
- Injuries
- 29,356
- Malfunctions
- 20,961
Reports per year
2,41712
2,48213
3,00214
3,72415
3,03016
3,29317
3,97818
3,92619
2,77620
2,86921
2,94722
4,46823
3,39624
3,42025
1,93326
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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