Unomedical Devices S.A. DE C.V.
FDA adverse event reports naming Unomedical Devices S.A. DE C.V. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: UNOMEDICAL DEVICES S.A. DE C.V..
- Total reports
- 14,273
- Deaths
- 17
- Injuries
- 4,594
- Malfunctions
- 9,662
Reports per year
711
512
5213
123
524
9,69125
4,51226
Source: FDA adverse event reports by year received, 2011–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA14,211
- Cystometric Gas (Carbon-Dioxide) On Hydraulic DeviceFAP38
- Non-Invasive Central Venous ManometerPFA17
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ2
- Board, BedFPS2
- Ventilator, Emergency, Manual (Resuscitator)BTM1
- Loupe, Diagnostic/SurgicalFSP1
- Pump, Infusion, InsulinLZG1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Unomedical Devices S.A. DE C.V. automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.