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
- 2,918
- Deaths
- 7
- Injuries
- 302
- Malfunctions
- 2,591
Reports per year
402
52703
38304
75305
65306
55707
3808
209
110
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 SurgicalLFL789
- Laparoscope, General & Plastic SurgeryGCJ387
- Stapler, SurgicalGAG334
- Applier, Surgical, ClipGDO279
- Product code KOGKOG259
- Staple, ImplantableGDW249
- Clip, ImplantableFZP188
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI179
- Instrument, BiopsyKNW172
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS29
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.