GE Healthcare recalls NM/CT 860 system model H3908AD due to loose rotor bearing screws that may cause a bearing to release during use, posing a risk of injury. Affected units have specific serial numbers listed.
GE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.
GE Healthcare is recalling its NM/CT 860 system model H3908AD because loose rotor bearing screws could cause one of the four rotor bearings to release during operation. This poses a risk of injury to users, especially during medical imaging procedures.
Loose rotor bearing screws in the detector could cause one of the four rotor bearings to release during operation. This might lead to equipment malfunction or injury if the bearing dislodges unexpectedly during imaging procedures.
Medical facilities using the GE NM/CT 860 system model H3908AD with the listed serial numbers are most at risk. Patients undergoing nuclear medicine imaging procedures may also be affected if the equipment malfunctions.
Check if your GE NM/CT 860 system has the model number H3908AD and one of the listed serial numbers: 860Y62012 through 860Z62033.
Verify your unit's serial number against the list: 860Y62012, 860Y62013, 860Y62015, 860Y62016, 860Y62017, 860Y62018, 860Y62019, 860Z62031, 860Z62032, 860Z62033.
The recalled model number is H3908AD for the GE NM/CT 860 system.
Loose rotor bearing screws could cause one of the four rotor bearings to release during operation, potentially leading to injury.
Check your serial number against the list: 860Y62012 through 860Z62033.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0854-2021 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0854-2021 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.
