GE Healthcare recalls specific models of Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma Camera H3000ZL Acquisition Systems due to risk of detector detachment and falling. Affected units have unique system IDs listed in the recall notice.
A detector can detach and fall.
GE Healthcare is recalling certain models of their Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma Camera H3000ZL Acquisition Systems because a detector can detach and fall. This hazard could lead to injury if the detector falls on someone.
The detector in this gamma camera can become detached and fall from the system. If it falls, it could cause injury to people nearby, such as staff or patients in the medical facility.
Medical facilities that use this specific gamma camera system are most at risk. Patients and staff using the affected models could be injured if the detector falls.
Check the system ID numbers listed in the recall notice. Affected models include specific system IDs like 334428MG, 256235NM2, and many others listed in the recall notice.
Identify your system ID by checking the label on the camera or the documentation provided with the unit.
If your system ID matches the list in the recall, contact GE Healthcare for further instructions.
A detector can detach and fall from the system, which could cause injury if it falls on someone nearby.
Check the system ID on your camera. Affected models have specific IDs listed in the recall notice, such as 334428MG or 256235NM2.
Contact GE Healthcare directly to confirm if your system is affected and follow their 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-0370-2019 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0370-2019 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.
