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.