GE Healthcare recalls Discovery NM 630 MRI systems with model H3101RH due to loose rotor bearing screws that could cause system failure.
Rotor bearing screws were found loose on detector.
GE Healthcare is recalling certain Discovery NM 630 MRI systems with model number H3101RH because loose rotor bearing screws could lead to system failure. This recall affects medical facilities using these specific machines.
Loose rotor bearing screws in the MRI system could cause the machine to malfunction or stop working during operation. This might lead to system failure but does not pose an immediate risk of injury to users.
Medical facilities that own or use the Discovery NM 630 MRI system with model number H3101RH are affected. Hospital staff and technicians who operate these systems are most at risk.
Check for the model number H3101RH on the system's label. The recall includes specific serial numbers and system IDs listed in the official notice.
Verify the model number and serial numbers listed in the official recall notice to confirm if your system is affected.
The recall indicates loose rotor bearing screws that could cause system failure, but it does not pose an immediate risk of injury to users.
Check for the model number H3101RH and the specific serial numbers or system IDs listed in the official recall notice.
The recall does not specify a remedy, so contact GE Healthcare directly for further instructions.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2994-2020 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2994-2020 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.
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.
