QEXClass 2
Coronary Mechanical Thrombectomy With Aspiration
FDA adverse event reports and recall history for coronary mechanical thrombectomy with aspiration (product code QEX), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 211
- Deaths
- 0
- Injuries
- 29
- Malfunctions
- 182
Reports per year
619
3020
8121
1622
2523
2524
2425
426
Source: FDA adverse event reports by year received, 2019–2026. 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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