Siemens recalls AXIOM Luminos TF, Iconos R100 and R200 models due to potential footrest detachment during use. Affected units have specific material numbers and serials; contact for remedy.
There is potential for the footrest to detach from the patient table during use.
Siemens is recalling several MRI scanner models because the footrest might detach from the patient table while in use. This could lead to injury if the footrest falls on the patient. Affected units have specific material numbers and serials listed in the recall.
The footrest on these MRI scanners may become loose and detach from the patient table during use. If it falls, it could strike a patient or cause injury. This risk is higher during scans when the table is moving.
Healthcare facilities using Siemens MRI scanners with the listed models and material numbers are most at risk. Patients and staff during scans could be affected if the footrest detaches.
Check for the specific material numbers listed: 10093902 for Luminos TF, 05895151 for R100, 10093961 for R200 C69, 10093962 for R200 C20, and 10094200 for dRF. These models were sold with no UDI (Unique Device Identification).
Identify if your scanner matches the listed models and material numbers in the recall notice.
The footrest on these MRI scanners may detach from the patient table during use, posing a risk of injury to patients or staff.
Check for the specific material numbers listed: 10093902 for Luminos TF, 05895151 for R100, 10093961 for R200 C69, 10093962 for R200 C20, and 10094200 for dRF.
The recall does not specify a remedy; contact Siemens directly for further instructions.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1000-2023 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1000-2023 from Siemens. 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.
