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/AEMS corpus and the live FDA recall database.
- Total reports
- 51,947
- Deaths
- 1,855
- Injuries
- 29,201
- Malfunctions
- 20,858
Reports per year
2,41712
2,48213
3,00214
3,72415
3,02916
3,29317
3,97818
3,92619
2,77620
2,86921
2,94722
4,46823
3,39624
3,42025
1,67426
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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