MFAClass 3
Device, Removal, Pacemaker Electrode, Percutaneous
FDA adverse event reports and recall history for device, removal, pacemaker electrode, percutaneous (product code MFA), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 1,555
- Deaths
- 508
- Injuries
- 922
- Malfunctions
- 115
Reports per year
13412
14213
12114
7315
9116
9617
7718
6619
7720
8321
6022
5523
7024
6825
7926
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.
Monitor device, removal, pacemaker electrode, percutaneous automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.