JYSClass 1
Perforator, Ear-Lobe
FDA adverse event reports and recall history for perforator, ear-lobe (product code JYS), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 393
- Deaths
- 0
- Injuries
- 2
- Malfunctions
- 0
Reports per year
3397
8898
6999
6500
4001
2802
2003
1604
2005
906
507
Source: FDA adverse event reports by year received, 1997–2007. 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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