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 BRIVO B615 variants 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 that could have a detector fall risk if not properly installed. This could lead to serious injury if the detector falls during use.
The detector may not be correctly installed, which can cause it to fall. If the detector falls, it could cause serious injury to people nearby.
Healthcare facilities using the recalled GE Nuclear Medicine 600/800 series systems are most at risk. Patients and staff using these systems could be affected if the detector falls.
Check for the specific models listed: BRIVO B615 3/8 inch DHP BJG NR, BRIVO 615 3/8 inch, or other variants with serial numbers starting with NT2QG or 00000168527HL0.
Identify if your system matches the listed models and serial numbers in the recall notice.
The detector may not be correctly installed, which can cause it to fall and lead to life-threatening injury.
BRIVO B615 3/8 inch DHP BJG NR, BRIVO 615 3/8 inch, and other variants with specific serial numbers starting with NT2QG or 00000168527HL0.
The recall does not require immediate stop use; however, you should check if your system is affected and follow the action 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-1055-2023 — GE Medical Systems Israel GE Medical Systems Israel Hello, I own a GE Medical Systems Israel that is covered by recall Z-1055-2023 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.
