GE Healthcare recalls NM/CT 850 Model H3907AD with loose rotor bearing screws that could cause equipment 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/CT 850 models due to loose rotor bearing screws that could lead to equipment malfunction. This recall affects medical imaging devices used in healthcare settings where proper operation is critical.
Loose rotor bearing screws in the detector could cause equipment failure during operation. This might lead to inaccurate imaging results or temporary shutdowns, but the recall indicates no immediate risk of injury or serious harm.
Healthcare facilities and medical professionals using GE Healthcare NM/CT 850 models with specific serial numbers and system IDs listed in the recall notice. Patients and staff at these facilities are at risk if the equipment malfunctions.
Check for the model number H3907AD on the device and specific serial numbers listed in the recall notice, such as 85EX67001, 85EX67023, and others with corresponding system IDs.
Identify the model number and serial number on your GE Healthcare NM/CT 850 device to confirm if it is affected by this recall.
GE Healthcare found loose rotor bearing screws on certain NM/CT 850 models that could cause equipment failure.
Check your device's model number (H3907AD) and serial number against the list of affected units provided in the 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-2991-2020 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2991-2020 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.
