GE Healthcare recalls NM 830 Model H3910AC MRI systems 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 NM 830 MRI systems with model number H3910AC due to loose rotor bearing screws. This could lead to system malfunction or failure if the screws become dislodged during operation.
Loose rotor bearing screws in the MRI system could become dislodged during operation, potentially causing system failure. This might lead to the machine not functioning properly or causing damage to the equipment.
Owners of GE Healthcare NM 830 MRI systems with model number H3910AC and specific serial numbers listed in the recall notice are affected. Medical facilities using these systems are most at risk.
Check if your GE Healthcare NM 830 MRI system has model number H3910AC and one of the listed serial numbers or system IDs in the recall notice. The specific serial numbers and system IDs are provided in the recall documentation.
Verify your MRI system's model number and serial number against the list of affected units provided in the recall notice.
GE Healthcare found loose rotor bearing screws on certain NM 830 MRI systems, which could lead to system failure if dislodged during operation.
Check your unit's model number (H3910AC) and serial number against the list of affected units provided in the recall notice.
The recall notice 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-2995-2020 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2995-2020 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.
