LNKClass 2
Laser For Gastro-Urology Use
FDA adverse event reports and recall history for laser for gastro-urology use (product code LNK), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 186
- Deaths
- 3
- Injuries
- 49
- Malfunctions
- 111
Reports per year
899
200
202
203
404
1805
2506
2407
1508
809
410
111
113
221
223
Source: FDA adverse event reports by year received, 1999–2023. 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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