EKXClass 1
Handpiece, Direct Drive, Ac-Powered
FDA adverse event reports and recall history for handpiece, direct drive, ac-powered (product code EKX), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 736
- Deaths
- 0
- Injuries
- 54
- Malfunctions
- 677
Reports per year
2712
4513
10214
6815
6616
1017
4918
5619
6720
7921
3722
1423
1924
925
1326
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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