QMGClass 3
Shockwave Intravascular Lithotripsy System
FDA adverse event reports and recall history for shockwave intravascular lithotripsy system (product code QMG), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 432
- Deaths
- 97
- Injuries
- 241
- Malfunctions
- 92
Reports per year
2121
5722
6323
11324
13025
4826
Source: FDA adverse event reports by year received, 2021–2026. 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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