LNSClass 2
Lithotriptor, Extracorporeal Shock-Wave, Urological
FDA adverse event reports and recall history for lithotriptor, extracorporeal shock-wave, urological (product code LNS), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 811
- Deaths
- 30
- Injuries
- 569
- Malfunctions
- 171
Reports per year
2012
1813
2114
2215
5016
5417
5918
6019
3820
5521
5222
8623
4024
6125
1626
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
- TerminatedSoftware design
MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.
Display freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user.
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