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
- 12,392
- Deaths
- 43
- Injuries
- 1,233
- Malfunctions
- 11,049
Reports per year
1302
1,72103
2,23104
1,70205
1,95606
4,04407
63708
8309
510
Source: FDA adverse event reports by year received, 2002–2010. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Instrument, Ultrasonic SurgicalLFL3,030
- Staple, ImplantableGDW1,552
- Laparoscope, General & Plastic SurgeryGCJ1,525
- Clip, ImplantableFZP1,241
- Stapler, SurgicalGAG1,155
- Applier, Surgical, ClipGDO1,123
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI868
- Product code KOGKOG832
- Instrument, BiopsyKNW739
- Instrument, Manual, Surgical, General UseMDM56
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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