JDNClass 2
Implant, Fixation Device, Spinal
FDA adverse event reports and recall history for implant, fixation device, spinal (product code JDN), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 909
- Deaths
- 6
- Injuries
- 616
- Malfunctions
- 205
Reports per year
510
311
812
6413
1714
2315
216
617
218
619
620
221
1622
823
124
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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