Covidien Surgical
FDA adverse event reports naming Covidien Surgical as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN SURGICAL.
- Total reports
- 6,608
- Deaths
- 24
- Injuries
- 535
- Malfunctions
- 6,049
Reports per year
110
111
112
213
219
220
323
2124
3,19725
3,37826
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Staple, ImplantableGDW3,705
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM2,441
- Stapler, SurgicalGAG183
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT76
- Laparoscope, General & Plastic SurgeryGCJ74
- Modular Electromechanical Surgical SystemSCV49
- Mesh, Surgical, PolymericFTL37
- Suture, Nonabsorbable, Synthetic, PolyamideGAR18
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW9
- Endoscopic Tissue Approximation DeviceOCW5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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