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
- 8,157
- Deaths
- 14
- Injuries
- 534
- Malfunctions
- 7,572
Reports per year
402
14903
99104
1,67405
1,54706
1,72807
72008
1,34309
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 SurgicalLFL2,561
- Clip, ImplantableFZP942
- Staple, ImplantableGDW827
- Laparoscope, General & Plastic SurgeryGCJ799
- Applier, Surgical, ClipGDO729
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI627
- Stapler, SurgicalGAG576
- Instrument, BiopsyKNW500
- Product code KOGKOG439
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS32
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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