Samsung Digital Diagnostic Mobile X-ray System Model GM85 (UDI-DI: 08806088582412) may have arm frame welding issues causing potential falls that could harm users. Affected units include specific serial numbers listed in the recall.
Mobile x-ray systems moving arm frame welding issue which presents the potential of bodily harm due to fall of the arm.
Samsung Digital Diagnostic Mobile X-ray System Model GM85 units with certain serial numbers have a welding issue in the arm frame that could cause the arm to fall, potentially leading to bodily harm. This recall affects medical facilities using these specific models.
The mobile x-ray system's arm frame has a welding issue that may cause it to fall during use. This could result in bodily harm to the person operating the device or nearby individuals.
Medical facilities that own or use the Samsung Digital Diagnostic Mobile X-ray System Model GM85 with the listed serial numbers are most at risk. Patients and staff using these units could be affected if the arm frame falls.
Check if your unit has the Samsung Digital Diagnostic Mobile X-ray System Model GM85 with the specific serial numbers listed in the recall notice. The UDI-DI code is 08806088582412.
Verify if your unit has one of the listed serial numbers from the recall notice.
Reach out to NeuroLogica Corporation for further assistance with the recall.
The recalled model is Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
Check if your unit has a serial number listed in the provided recall notice.
Contact NeuroLogica Corporation to confirm if your unit is affected and follow their instructions.
We’ve drafted a message you can send Samsung to request your refund or repair — edit it as you like.
Subject: Recall Z-1056-2024 — Samsung Samsung Hello, I own a Samsung that is covered by recall Z-1056-2024 from Samsung. 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.
