LWFClass 1
Dilator, Nasal
FDA adverse event reports and recall history for dilator, nasal (product code LWF), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 216
- Deaths
- 2
- Injuries
- 145
- Malfunctions
- 7
Reports per year
410
911
1212
1013
1214
4115
3916
1317
1518
1319
620
421
522
223
824
Source: FDA adverse event reports by year received, 2010–2024. 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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