Covidien Ag Juarez (mmj)
FDA adverse event reports naming Covidien Ag Juarez (mmj) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN AG JUAREZ (MMJ).
- Total reports
- 2,652
- Deaths
- 12
- Injuries
- 283
- Malfunctions
- 2,357
Reports per year
119
3620
3221
5622
4623
29824
1,40825
77526
Source: FDA adverse event reports by year received, 2019–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Tube, Tracheal (W/Wo Connector)BTR1,873
- Tube Tracheostomy And Tube CuffJOH586
- Esophageal Dilator Balloon With Or Without Electrode SensorsPID99
- Laryngoscope, RigidCCW19
- System, Gastrointestinal Motility (Electrical)FFX17
- Continuous Measurement ThermometerFLL14
- Esophagoscope (Flexible Or Rigid)EOX12
- Stylet, Tracheal TubeBSR10
- Airway, NasopharyngealBTQ9
- Esophageal Dilator With Balloon And Electrode SensorsPIE5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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