PlainRecalls
FDA Devices Moderate Class II Ongoing

GE Proteus XR/A radiographic system

Reported: December 4, 2024 Initiated: October 24, 2024 #Z-0550-2025

Product Description

GE Proteus XR/A radiographic system

Reason for Recall

Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by GE HealthCare have not been replaced at the intervals detailed in the Preventative Maintenance Action List.

Details

Units Affected
956 systems
Distribution
Worldwide - US Nationwide distribution.
Location
Beijing

Frequently Asked Questions

What product was recalled?
GE Proteus XR/A radiographic system. Recalled by GE Healthcare (China) Co., Ltd.. Units affected: 956 systems.
Why was this product recalled?
Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by GE HealthCare have not been replaced at the intervals detailed in the Preventative Maintenance Action List.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 4, 2024. Severity: Moderate. Recall number: Z-0550-2025.