Covidien MFG Solutions S.A.
FDA adverse event reports naming Covidien MFG Solutions S.A. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN MFG SOLUTIONS S.A..
- Total reports
- 2,400
- Deaths
- 53
- Injuries
- 359
- Malfunctions
- 1,988
Reports per year
20117
35118
28619
31920
37321
46022
35723
5324
Source: FDA adverse event reports by year received, 2017–2024. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Hemodialysis, ImplantedMSD904
- Catheter, Peritoneal, Long-Term IndwellingFJS525
- Catheter, Hemodialysis, Non-ImplantedMPB405
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ307
- Catheter, Hemodialysis, Triple Lumen, Non-ImplantedNIE130
- Catheter, SubclavianLFJ42
- Catheter, Hemodialysis, Implanted, CoatedNYU39
- Kit, Repair, Catheter, HemodialysisNFK17
- Catheter, Peritoneal Dialysis, Single UseFKO6
- Catheter, Umbilical ArteryFOS6
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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