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 corpus and the live FDA recall database.
- Total reports
- 1,561
- Deaths
- 510
- Injuries
- 926
- Malfunctions
- 115
Reports per year
13412
14213
12114
7315
9116
9617
7718
6619
7720
8321
6022
5523
7024
6825
8526
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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