Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GE Brivo OEC715/785/865 C-Arm Recalled by GE Healthcare Beijing , Hangwei Medical Systems, Co. LTD Due to GE is recalling certain lots of GE Brivo...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Healthcare Beijing , Hangwei Medical Systems, Co. LTD directly.
Affected Products
GE Brivo OEC715/785/865 C-Arm, Models: 715 Prime, 785 Essential, and 865 Plus. The QEC 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.
Quantity: 29
Why Was This Recalled?
GE is recalling certain lots of GE Brivo OEC715/785/865 C-Arm due to the potential for the wires in the high voltage cable bundle to fail, resulting in loss of system functionality.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Healthcare Beijing , Hangwei Medical Systems, Co. LTD
GE Healthcare Beijing , Hangwei Medical Systems, Co. LTD has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report