GE OEC Medical Systems recalls

GE OEC Medical Systems has 47 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 25 Dec 2024. 9 are still ongoing.

Total recalls47since 2012
Last 12 months0reported
Class I511% of total
Ongoing9latest 25 Dec 2024

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 5 11%Class II 42 89%Class III 0 0%

Why ge oec medical systems is recalled

By year

Ongoing ge oec medical systems recalls

9 active

All ge oec medical systems recalls, newest first

47 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIOEC 9800 REF Image-Intensified Fluoroscopic X-Ray System recalledGE OEC Medical SystemsPackaging Defects44 states
DeviceCLASS IIOEC 9900 REF Image-Intensified Fluoroscopic X-Ray System recalledGE OEC Medical SystemsPackaging Defects44 states
DeviceCLASS IIOEC Elite recalled by GE OEC Medical SystemsGE OEC Medical SystemsPackaging Defects44 states
DeviceCLASS IIOEC 3D recalled by GE OEC Medical SystemsGE OEC Medical SystemsPackaging Defects44 states
DeviceCLASS IIOEC Elite Systems with Image Intensifier recalledGE OEC Medical SystemsOtherNationwide
DeviceCLASS IIOEC 9800 Systems with Image Intensifier recalledGE OEC Medical SystemsOtherNationwide
DeviceCLASS IIOEC 9900 Systems with Image Intensifier recalledGE OEC Medical SystemsOtherNationwide
DeviceCLASS IIField Upgrade Kits recalled by GE OEC Medical SystemsGE OEC Medical SystemsOtherNationwide
DeviceCLASS IIOEC Flexiview 8800 Systems with Image Intensifier recalledGE OEC Medical SystemsOtherNationwide
DeviceCLASS IIOEC Elite mobile C-arm recalled by GE OEC Medical SystemsGE OEC Medical SystemsTemperature AbuseNationwide
DeviceCLASS IIOEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile recalledGE OEC Medical SystemsTemperature AbuseNationwide
DeviceCLASS IIOEC FlexiView 8800, Digital Mobile Imaging System recalledGE OEC Medical SystemsDevice MalfunctionCA
DeviceCLASS IIOEC 9800. MDL Numbers: D222250, D141598 recalledGE OEC Medical SystemsOtherVA
DeviceCLASS IIOEC 9900 Elite recalled by GE OEC Medical SystemsGE OEC Medical SystemsOtherVA
DeviceCLASS IIThe OEC 9900 Elite mobile fluoroscopy system is designed recalledGE OEC Medical SystemsDevice Malfunction50 states
DeviceCLASS IIOEC MiniView recalled by GE OEC Medical SystemsGE OEC Medical SystemsDevice Malfunction50 states
DeviceCLASS IIOEC 9800. MDL Numbers: D222250 recalled by GE OEC Medical SystemsGE OEC Medical SystemsDevice Malfunction50 states
DeviceCLASS IIOEC Brivo 785 Essential recalled by GE OEC Medical SystemsGE OEC Medical SystemsOtherNationwide
DeviceCLASS IIOEC 9800, fluoroscopic x-ray system recalled by GE OEC Medical SystemsGE OEC Medical SystemsOtherNationwide
DeviceCLASS IIOEC UroView 2800, fluoroscopic x-ray system recalledGE OEC Medical SystemsOtherNationwide
DeviceCLASS IIGE OEC Brivo 865 plus, Mobile X-ray system laser aimer assemblies recalledGE OEC Medical SystemsOther6 states
DeviceCLASS IIGE OEC Brivo 715 Prime Mobile C-Arm X-Ray Product Used recalledGE OEC Medical SystemsProcessing DeviationUT
DeviceCLASS IIGE OEC Brivo 865 Plus Mobile C-Arm X-Ray Product Used recalledGE OEC Medical SystemsProcessing DeviationUT
DeviceCLASS IIOEC¿ MiniView recalled by GE OEC Medical SystemsGE OEC Medical SystemsOtherUT
DeviceCLASS IIOEC¿ UroView recalled by GE OEC Medical SystemsGE OEC Medical SystemsOtherUT
DeviceCLASS IISeries OEC recalled by GE OEC Medical SystemsGE OEC Medical SystemsOtherUT
DeviceCLASS IIFlexiView 8800 Digital Mobile Imaging System recalledGE OEC Medical SystemsOtherUT
DeviceCLASS IIThe OEC 9900 Elite mobile fluoroscopy system recalledGE OEC Medical SystemsOtherUT
DeviceCLASS IIInstaTrak¿ 3500 Plus, ENTrakTM Plus, InstaTrak¿ recalledGE OEC Medical SystemsOtherNationwide
DeviceCLASS IOEC IT3000; IT2500 (EnTrak); IT2500 Plus (EnTrak Plus) recalledGE OEC Medical SystemsOtherNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.