GE Medical recalls Discovery XR656HD X-ray systems where users may continue scanning after automatic exposure limits are reached, risking overexposure without warning.
The user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure techniques. In all cases, a message still appears on the screen when the AEC limit is reached.
GE Medical is recalling its Discovery XR656HD X-ray imaging systems because users might take additional scans after the automatic exposure limit is reached, potentially leading to overexposure without further action. This could cause unnecessary radiation exposure to patients or staff.
The system allows users to continue taking scans after the automatic exposure control limit is reached, without requiring any action to adjust exposure. A warning message appears on the screen, but users might miss it or not realize they need to stop scanning.
Healthcare facilities using the Discovery XR656HD X-ray system are most affected, particularly radiology staff and patients who may be exposed to unnecessary radiation during imaging procedures.
The recalled product is the Discovery XR656HD X-ray imaging system. It was sold with GTINs 00840682142175 and 00840682142168.
Look for the warning message on the screen when the automatic exposure limit is reached to confirm if the system is functioning correctly.
The recall indicates a potential risk of unnecessary radiation exposure if users continue scanning after the automatic exposure limit is reached, but the hazard is not severe enough to require immediate discontinuation.
The official recall notice does not specify a remedy, so users should check the system status and contact GE Medical Systems for further guidance.
The recalled system is the Discovery XR656HD X-ray imaging system with GTINs 00840682142175 and 00840682142168.
We’ve drafted a message you can send GE Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1044-2025 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-1044-2025 from GE Medical Systems. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
