ISNClass 1
Cable
FDA adverse event reports and recall history for cable (product code ISN), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 122
- Deaths
- 0
- Injuries
- 11
- Malfunctions
- 106
Reports per year
108
1009
2810
211
612
1213
714
1915
216
417
618
719
420
324
325
Source: FDA adverse event reports by year received, 2008–2025. 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.
Monitor cable automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.