GE Medical Systems Israel recalls specific GE Nuclear Medicine 600/800 series systems due to potential detector fall causing life-threatening injury. Affected models include 870, 870 DR variants, and D670 series with certain serial numbers.
A mitigation may not be correctly implemented. If this is the case, the detector can fall, leading to life-threatening bodily injury.
GE Medical Systems Israel is recalling specific nuclear medicine imaging systems (870 and D670 series) because a faulty mitigation may cause the detector to fall, leading to serious injury. This affects systems with certain serial numbers and configurations.
The recall states that if the mitigation (a safety feature) is not correctly implemented, the detector can fall. This falling detector poses a risk of causing serious injury, including life-threatening harm to users.
Healthcare facilities and medical professionals using the recalled GE Nuclear Medicine 600/800 series systems are most at risk. The hazard could cause life-threatening injury if the detector falls during operation.
Check if your system is listed in the detailed model descriptions and serial numbers provided in the recall notice. The affected models include 870, 870 DR variants, and D670 series with specific serial numbers and configurations.
Immediately stop using the recalled GE Nuclear Medicine 600/800 series systems as they may cause the detector to fall, leading to serious injury.
The recall affects GE Nuclear Medicine 600/800 series systems including 870 models, 870 DR variants, and D670 series with specific serial numbers and configurations as listed in the detailed model descriptions.
Check your system's model and serial numbers against the detailed list of affected models and serial numbers provided in the recall notice.
Immediately stop using the affected system and contact GE Medical Systems Israel for further instructions.
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-1053-2023 — GE Medical Systems Israel GE Medical Systems Israel Hello, I own a GE Medical Systems Israel that is covered by recall Z-1053-2023 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.
