Ethicon Endo Surgery, Inc.(cincinnati)
FDA adverse event reports naming Ethicon Endo Surgery, Inc.(cincinnati) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ETHICON ENDO SURGERY, INC.(CINCINNATI).
- Total reports
- 2,667
- Deaths
- 0
- Injuries
- 146
- Malfunctions
- 2,505
Reports per year
4403
40604
91105
1,02506
27907
108
110
Source: FDA adverse event reports by year received, 2003–2010. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Instrument, Ultrasonic SurgicalLFL919
- Laparoscope, General & Plastic SurgeryGCJ286
- Stapler, SurgicalGAG283
- Applier, Surgical, ClipGDO253
- Clip, ImplantableFZP199
- Product code KOGKOG184
- Instrument, BiopsyKNW175
- Staple, ImplantableGDW172
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI124
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS31
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Ethicon Endo Surgery, Inc.(cincinnati) 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.