GE Healthcare Discovery NM/CT 670 PRO models with specific serial numbers may have been moved without proper detector support, risking detector falls and serious injury. Affected units include models H2401AK, H2402AC, H3100AH, H3100XB, and 5376204-70-54-2.
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 is recalling certain Discovery NM/CT 670 PRO medical imaging systems that could have been moved without proper detector support. This might cause the detector to fall, leading to serious injury or death. Affected units have specific model and serial numbers listed in the recall.
If the system is moved or relocated without proper detector support, excessive force can be applied to the detector mounting. This may cause the detector to fall, potentially leading to serious injury or death.
Healthcare facilities that own or use these specific medical imaging systems are most at risk. Patients and staff could be injured if the detector falls during use.
Check for model numbers H2401AK, H2402AC, H3100AH, H3100XB, or 5376204-70-54-2. The serial numbers listed in the recall details will help identify affected units.
Identify your system using the model numbers listed: H2401AK, H2402AC, H3100AH, H3100XB, or 5376204-70-54-2.
Reach out to GE Medical Systems Israel to confirm if your specific serial number is affected.
GE Healthcare has identified that certain Discovery NM/CT 670 PRO systems could have been moved without proper detector support, which might cause the detector to fall and lead to serious injury.
Check your model and serial number against the list provided in the recall. Contact GE Medical Systems Israel to confirm if your unit is affected.
Yes, if the detector falls during use, it could cause serious injury or death. Proper detector support is needed during movement to prevent this.
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-0893-2025 — GE Medical Systems Israel GE Medical Systems Israel Hello, I own a GE Medical Systems Israel that is covered by recall Z-0893-2025 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.
