GE Healthcare recalls certain Infinia II nuclear medicine systems (model numbers H2799ZP and H3000WT) that could have been moved without proper detector support, potentially causing detector falls and serious injury.
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 specific Infinia II nuclear medicine systems (model numbers H2799ZP and H3000WT) because they could have been transported or relocated without proper detector support. This might cause excessive load on detector mounting mechanisms, leading to detector falls and life-threatening injuries.
The detector mounting mechanisms in these systems could experience excessive load if the system is moved or relocated without proper detector support. This might cause the detector to fall, potentially resulting in serious injury or death.
Healthcare facilities and medical professionals who own or use the recalled Infinia II systems (model numbers H2799ZP and H3000WT) are most at risk. The hazard occurs during transportation or relocation without proper detector support.
Check for the model numbers H2799ZP or H3000WT on the system. These are specific Infinia II nuclear medicine systems that could be affected by improper handling during transport or relocation.
Identify the system model number (H2799ZP or H3000WT) to confirm if it is affected.
Reach out to GE Healthcare for further instructions on how to address the issue.
The affected models are H2799ZP and H3000WT for the Infinia II nuclear medicine systems.
If the system is moved or relocated without proper detector support, it could cause excessive load on the detector mounting mechanisms, potentially leading to a detector fall and serious injury.
Check your system model number and contact GE Healthcare for specific instructions on how to address the issue.
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-0897-2025 — GE Medical Systems Israel GE Medical Systems Israel Hello, I own a GE Medical Systems Israel that is covered by recall Z-0897-2025 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.
