Covidien, Formerly Tyco Healthcare
FDA adverse event reports naming Covidien, Formerly Tyco Healthcare as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN, FORMERLY TYCO HEALTHCARE.
- Total reports
- 1,124
- Deaths
- 18
- Injuries
- 657
- Malfunctions
- 442
Reports per year
207
11408
23209
32210
11911
19512
12413
1614
Source: FDA adverse event reports by year received, 2007–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Tube Tracheostomy And Tube CuffJOH375
- OximeterDQA293
- Tube, Tracheostomy (W/Wo Connector)BTO206
- Tube, Tracheal (W/Wo Connector)BTR168
- Tube, Bronchial (W/Wo Connector)BTS24
- System, Thermal RegulatingDWJ14
- Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)CBI12
- Oximeter, EarDPZ8
- Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK6
- Oximeter, ReprocessedNLF5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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