MMJ Sa DE CV (usd)
FDA adverse event reports naming MMJ Sa DE CV (usd) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MMJ SA DE CV (USD).
- Total reports
- 6,502
- Deaths
- 67
- Injuries
- 1,365
- Malfunctions
- 5,070
Reports per year
116
51317
32118
58919
67920
78621
1,03022
1,07223
1,40924
10225
Source: FDA adverse event reports by year received, 2016–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Tube, Tracheal (W/Wo Connector)BTR3,616
- Tube Tracheostomy And Tube CuffJOH2,342
- Index-Generating Electroencephalograph SoftwareOLW131
- Laryngoscope, RigidCCW118
- Oximeter, Tissue SaturationMUD86
- Tube, Tracheostomy (W/Wo Connector)BTO54
- System, Thermal RegulatingDWJ51
- OximeterDQA36
- Stylet, Tracheal TubeBSR22
- Continuous Measurement ThermometerFLL8
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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