NQWClass 2
Orthosis, Spine, Plate, Laminoplasty, Metal
FDA adverse event reports and recall history for orthosis, spine, plate, laminoplasty, metal (product code NQW), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 200
- Deaths
- 0
- Injuries
- 75
- Malfunctions
- 125
Reports per year
112
4913
514
1115
716
1917
518
819
220
721
1622
523
1524
3325
1526
Source: FDA adverse event reports by year received, 2012–2026. 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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