NZKClass 3
Stimulator, Low Electric Field, Tumor Treatment
FDA adverse event reports and recall history for stimulator, low electric field, tumor treatment (product code NZK), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 767
- Deaths
- 27
- Injuries
- 724
- Malfunctions
- 1
Reports per year
1212
2213
1114
2315
916
1217
2318
2119
3020
3221
2622
2923
15624
24525
11626
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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