GE Healthcare Discovery NM/CT 670 models H2401BC, H2401CE, H2401CG, H3100AG, H3100JW, H3100NC may have been transported without proper detector support, risking detector falls and serious injury. Affected units include specific model numbers and serial numbers.
GE HealthCare has become aware that certain Infinia, VariCam/VG/VH, Brivo NM 615, Discovery NM 630, Discovery NM/CT 670, and Optima NM/CT 640 Nuclear Medicine systems (see Affected Products Details and Appendices) could have been transported or relocated without proper detector support, which can result in excessive load being applied to the detector mounting mechanisms. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
GE Healthcare Discovery NM/CT 670 systems with specific model numbers (H2401BC, H2401CE, H2401CG, H3100AG, H3100JW, H3100NC) could have been moved without proper detector support, potentially causing detector falls that lead to serious injury. Affected units are identified by model numbers and serial numbers.
The detector mounting mechanisms can become overloaded if the system is moved without proper support. This may cause the detector to fall, resulting in serious injury due to the weight and impact of the detector.
Medical facilities that own or use GE Healthcare Discovery NM/CT 670 systems with the listed model numbers and serial numbers are most at risk. These systems are used in nuclear medicine imaging and require proper handling to prevent detector falls.
Check if your GE Healthcare Discovery NM/CT 670 system has model numbers H2401BC, H2401CE, H2401CG, H3100AG, H3100JW, or H3100NC. Affected units also have specific serial numbers listed in the recall notice.
Verify your system's model number and serial number against the list provided in the recall notice to determine if it is affected.
Reach out to GE Healthcare for further assistance or to confirm if your system is affected and what steps to take.
The affected models are GE Healthcare Discovery NM/CT 670 with model numbers H2401BC, H2401CE, H2401CG, H3100AG, H3100JW, and H3100NC.
Check your system's model number and serial number against the list provided in the recall notice. Affected units have specific serial numbers listed for each model.
Contact GE Healthcare to confirm if your system is affected and to receive instructions on next steps.
We’ve drafted a message you can send GE Medical Systems Israel to request your refund or repair — edit it as you like.
Subject: Recall Z-0891-2025 — GE Medical Systems Israel GE Medical Systems Israel Hello, I own a GE Medical Systems Israel that is covered by recall Z-0891-2025 from GE Medical Systems Israel. 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.
