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GE OEC Medical Systems, Inc: Medical Device Recalls in 2016

Updated on March 25, 2026.

According to to data from the FDA, there were 3 medical device recalls made by GE OEC Medical Systems, Inc in 2016. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2012
2013
2014
2015
2016
2017
2021
2023
2024
  • OEC UroView 2800, fluoroscopic x-ray system
  • OEC 9800, fluoroscopic x-ray system
  • OEC Brivo 715 Prime, OEC Brivo 785 Essential, OEC Brivo 865 Advance Product Usage: The OEC Brivo Mobile C-Arm X-Ray Products are designed to provide digital spot film imaging and fluoroscopic image guidance for all adult and pediatric populations for orientations between patient anatomy and surgical instruments. The product is used for general surgical applications and musculoskeletal procedures to visualize, for example, implant localizations or needle positions for aspirations, injections or biopsy. The OEC Brivo is not indicated for interventional use.
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