Ethicon Endo-surgery, Inc. S.A. DE C.V.
FDA adverse event reports naming Ethicon Endo-surgery, Inc. S.A. DE C.V. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ETHICON ENDO-SURGERY, INC. S.A. DE C.V..
- Total reports
- 3,150
- Deaths
- 8
- Injuries
- 82
- Malfunctions
- 3,032
Reports per year
84298
2,30899
Source: FDA adverse event reports by year received, 1998–1999. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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