GE Healthcare recalls Discovery 670 DR Model H3100BT with loose rotor bearing screws that could cause system failure. Affected units have specific serial numbers and system IDs listed in the recall notice.
Rotor bearing screws were found loose on detector.
GE Healthcare is recalling certain Discovery 670 DR MRI systems with model number H3100BT due to loose rotor bearing screws. This could lead to system failure during operation, potentially causing safety risks for users.
Loose rotor bearing screws in the MRI system could lead to system failure during operation. This might cause the machine to malfunction, potentially affecting patient safety and imaging procedures.
Medical facilities that own or use the Discovery 670 DR MRI system with model number H3100BT and the listed serial numbers are affected. Hospital staff and patients using these systems are at risk if the issue causes system failure.
Check if your Discovery 670 DR MRI system has model number H3100BT and the specific serial numbers listed in the recall notice, including the corresponding system IDs.
Verify your system's serial number and system ID against the list provided in the recall notice to confirm if it is affected.
The recall is due to loose rotor bearing screws found in certain Discovery 670 DR MRI systems, which could lead to system failure during operation.
Check your system's serial number and system ID against the list of affected units provided in the recall notice.
The recall notice does not specify a remedy, so you should 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-2996-2020 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2996-2020 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.
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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.
