Covidien LP LLC North Haven
FDA adverse event reports naming Covidien LP LLC North Haven as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN LP LLC NORTH HAVEN.
- Total reports
- 47,485
- Deaths
- 185
- Injuries
- 7,048
- Malfunctions
- 40,252
Reports per year
4,24617
6,29318
7,21819
5,35720
5,41721
5,10622
5,43023
5,88224
2,53225
426
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Staple, ImplantableGDW38,929
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM5,638
- Laparoscope, General & Plastic SurgeryGCJ902
- Mesh, Surgical, PolymericFTL848
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT315
- Clip, ImplantableFZP217
- Stapler, SurgicalGAG217
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW93
- Agent, Absorbable Hemostatic, Non-Collagen BasedLMG49
- Suture, Nonabsorbable, Synthetic, PolyamideGAR37
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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