LWFClass 1
Dilator, Nasal
FDA adverse event reports and recall history for dilator, nasal (product code LWF), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 228
- Deaths
- 2
- Injuries
- 146
- Malfunctions
- 18
Reports per year
911
1212
1013
1214
4115
3916
1317
1518
1319
620
421
522
223
824
1226
Source: FDA adverse event reports by year received, 2011–2026. 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 dilator, nasal automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.