Class II

Medical Device Recall: GE Proteus XR/A radiographic system

GE Healthcare (China) Co., Ltd. · October 24, 2024

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.

Distribution

Worldwide - US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

956 systems

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0550-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

GE Healthcare (China) Co., Ltd. Medical Device Recall: GE Proteus XR/A radiographic system | SafeCheck