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
- 1,602
- Deaths
- 19
- Injuries
- 204
- Malfunctions
- 1,375
Reports per year
2204
905
11606
70307
16508
9209
11510
17311
3112
5213
3514
2415
4516
2017
Source: FDA adverse event reports by year received, 2004–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Staple, ImplantableGDW489
- Instrument, Ultrasonic SurgicalLFL371
- Clip, ImplantableFZP193
- Laparoscope, General & Plastic SurgeryGCJ132
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI129
- Applier, Surgical, ClipGDO125
- Instrument, BiopsyKNW80
- Stapler, SurgicalGAG14
- Staple, Removable (Skin)GDT14
- Product code KOGKOG13
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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