GE OEC Medical Systems (slc)
FDA adverse event reports naming GE OEC Medical Systems (slc) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: GE OEC MEDICAL SYSTEMS (SLC).
- Total reports
- 53,441
- Deaths
- 2
- Injuries
- 14
- Malfunctions
- 53,390
Reports per year
209
4,05810
10,68711
10,03712
11,40213
9,12214
4,00115
3,54416
58817
Source: FDA adverse event reports by year received, 2009–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, X-Ray, Fluoroscopic, Image-IntensifiedJAA46,639
- Interventional Fluoroscopic X-Ray SystemOWB6,108
- System, Image Processing, RadiologicalLLZ667
- Table, RadiologicKXJ13
- System, X-Ray, MobileIZL9
- Neurological Stereotaxic InstrumentHAW1
- System, X-Ray, AngiographicIZI1
- Solid State X-Ray Imager (Flat Panel/Digital Imager)MQB1
- Wearable Automated External DefibrillatorMVK1
- Image-Intensified Fluoroscopic X-Ray System, MobileOXO1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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