Covidien, Formerly US Surgical A Divison
FDA adverse event reports naming Covidien, Formerly US Surgical A Divison as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN, FORMERLY US SURGICAL A DIVISON.
- Total reports
- 3,041
- Deaths
- 34
- Injuries
- 1,283
- Malfunctions
- 1,703
Reports per year
35014
1,07515
1,39116
22517
Source: FDA adverse event reports by year received, 2014–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Staple, ImplantableGDW1,907
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM384
- Mesh, Surgical, PolymericFTL112
- Laparoscope, General & Plastic SurgeryGCJ111
- Mesh, SurgicalFTM89
- Instrument, Ultrasonic SurgicalLFL86
- Stapler, SurgicalGAG49
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS48
- Product code KOGKOG43
- Clip, ImplantableFZP34
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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