GE Medical Systems Israel recalls Discovery NM/CT 670 ES models with specific serial numbers due to potential detector fall risk from improper transport. Affected units may cause life-threatening injury if detector mounts are damaged.
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 Medical Systems Israel is recalling certain Discovery NM/CT 670 ES medical imaging systems because improper transport could damage detector mounts, leading to a detector falling and causing serious injury. This recall affects specific models with unique serial numbers.
Improper transport or relocation without proper detector support can cause excessive force on the detector mounting mechanisms. This may lead to the detector falling, which could cause serious injury or death to anyone nearby.
Medical facilities using the affected Discovery NM/CT 670 ES models are most at risk. Patients and staff could be injured if a detector falls during operation.
Check for the model number H3100XF on the system. Affected units have specific serial numbers listed in the recall notice, including T2AG12009/88227HL4 and others.
Identify your system's serial number from the list provided in the recall notice to confirm if it is affected.
Reach out to GE Medical Systems Israel for guidance on next steps if your system is affected.
The recall is due to potential detector falls from improper transport or relocation without proper detector support, which could cause serious injury.
The affected models are Discovery NM/CT 670 ES with model number H3100XF and specific serial numbers listed in the recall notice.
Check your system's serial number against the list of affected serial numbers provided in the recall notice.
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-0894-2025 — GE Medical Systems Israel GE Medical Systems Israel Hello, I own a GE Medical Systems Israel that is covered by recall Z-0894-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
