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
- 6,271
- Deaths
- 25
- Injuries
- 517
- Malfunctions
- 5,729
Reports per year
110
111
112
213
219
220
323
2124
3,19525
3,04326
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Staple, ImplantableGDW3,506
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM2,330
- Stapler, SurgicalGAG177
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT72
- Laparoscope, General & Plastic SurgeryGCJ69
- Modular Electromechanical Surgical SystemSCV41
- Mesh, Surgical, PolymericFTL38
- 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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