GKNClass 2
Timer, Clot, Automated
FDA adverse event reports and recall history for timer, clot, automated (product code GKN), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 327
- Deaths
- 0
- Injuries
- 8
- Malfunctions
- 319
Reports per year
315
217
119
120
1221
5422
12023
5424
5125
2926
Source: FDA adverse event reports by year received, 2015–2026. 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.
Monitor timer, clot, automated automatically
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