NQRClass 3
Sealant, Dural
FDA adverse event reports and recall history for sealant, dural (product code NQR), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 576
- Deaths
- 2
- Injuries
- 317
- Malfunctions
- 254
Reports per year
3312
3613
2614
2115
2316
2917
4518
3719
2420
2021
3922
1923
2024
5925
1426
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
No recalls listed in the FDA device recall database for this entry.
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