Splint, Intranasal Septal
FDA adverse event reports and recall history for splint, intranasal septal (product code LYA), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 202
- Deaths
- 3
- Injuries
- 103
- Malfunctions
- 88
Reports per year
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
- 2006-09-22TerminatedOther
Porex Nostril Retainers, CAT #7241, Size 4, Porex Surgical Inc., 15 Dart Road, Newnan, GA 30265 USA.
Device contains a trace amount of amine via introduction through an intermediate supplied by a third party raw material
- CompletedUnder Investigation by firm
ORCA FOAM STANDARD CUBE 10x10x10 mm, Absorbable Gelatin Sponge Hemostat, USP, REF ORCA FOAM
In routine bioburden testing, higher than acceptable levels of Endotoxins were observed.
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