GE Healthcare recalls certain Proteus XR/A radiographic systems where steel cables in the Wall Stand were not replaced per preventative maintenance schedules. Affected units have unique identifiers listed in the recall notice.
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.
GE Healthcare is recalling specific models of their Proteus XR/A radiographic systems because steel cables in the Wall Stand weren't replaced at the recommended maintenance intervals. This could lead to the cables failing during use, potentially causing equipment damage or injury.
The steel cables in the Wall Stand for certain Proteus XR/A systems were not replaced at the intervals specified in GE's Preventative Maintenance Action List. If these cables fail during use, they could cause the equipment to malfunction or become unstable, potentially leading to injury or damage.
Healthcare facilities that own or use GE Proteus XR/A radiographic systems with the specific model identifiers listed in the recall notice are most at risk. The hazard affects systems that have not been properly maintained according to GE's preventative maintenance schedule.
Check if your GE Proteus XR/A radiographic system has the unique identifiers listed in the recall notice, which include a specific sequence of numbers and letters starting with 'UDI-DI: 00840682120777' and system IDs like '907443PROTEUS 251847RAD 256737PRO' and others.
Identify if your system has the specific identifiers listed in the recall notice, such as UDI-DI: 00840682120777 and system IDs starting with 907443PROTEUS.
Reach out to GE Healthcare for guidance on whether your system is affected and what steps to take next.
The recall is happening because steel cables in the Wall Stand for certain Proteus XR/A systems were not replaced at the intervals detailed in GE's Preventative Maintenance Action List.
Your system is affected if it has the specific identifiers listed in the recall notice, including UDI-DI: 0084068120777 and system IDs starting with 907443PROTEUS.
Contact GE Healthcare to determine if your system is affected and follow their instructions for next steps.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0550-2025 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0550-2025 from GE Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
