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Open, Classified

GE Proteus XR/A radiographic system

FDA Recall Z-0550-2025 · Posted 2024-11-25

Recall StatusOpen, Classified
Product CodeKPR
Date Initiated2024-10-24
Product Quantity956 systems

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.

Firm Action

An URGENT MEDICAL DEVICE CORRECTION notification letter dated 10/24/24 was sent to customers. Actions to be taken by Customer/User " You can continue to use the system for table exams without limitations. " You can continue to use the wall stand for exams where the patient does not have any part of their body underneath the bucky. " Do not perform exams where the patient has any body part underneath the bucky until the Wall Stand steel cable has been inspected and if necessary, has been replaced. Please ensure all potential users in your facility are made aware of this safety notification and the recommended actions. Please retain this document for your records. Please complete and return the attached acknowledgement form to [email protected] GE HealthCare will correct all affected products at no cost to you. A GE HealthCare representative will contact you to arrange for the correction. If you have any questions or concerns regarding this notification, please contact GE HealthCare Service at 1-800-437-1171 or your local Service Representative.

Root Cause

Equipment maintenance

Distribution Pattern

Worldwide - US Nationwide distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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