Covidien (irvine)
FDA adverse event reports naming Covidien (irvine) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN (IRVINE).
- Total reports
- 3,679
- Deaths
- 265
- Injuries
- 1,653
- Malfunctions
- 1,761
Reports per year
413
3414
1,04915
77116
1,16517
58218
7419
Source: FDA adverse event reports by year received, 2013–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Intracranial Aneurysm Flow DiverterOUT1,305
- Agent, Injectable, EmbolicMFE710
- Device, Vascular, For Promoting EmbolizationKRD668
- Catheter, Thrombus RetrieverNRY362
- Catheter, Continuous FlushKRA345
- Catheter, Peripheral, AtherectomyMCW93
- Catheter, PercutaneousDQY71
- Catheter, Intravascular Occluding, TemporaryMJN47
- Wire, Guide, CatheterDQX37
- Device, Neurovascular EmbolizationHCG18
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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