Siemens Medical recalls ARTIS pheno, icono biplane, and icono floor models due to risk of tabletop detachment. Affected units have specific material and UDI/DI numbers. Contact for repair or replacement.
Mechanical connection between the tabletop and table base may be lost.
Siemens Medical is recalling three types of medical imaging equipment because the tabletop could become detached from the base. This poses a risk of injury during use, especially if the table is moved or adjusted.
The mechanical connection between the tabletop and table base may become loose or lose its connection. If this happens, the tabletop could detach while in use, potentially causing injury to patients or staff.
Medical facilities using the ARTIS pheno, icono biplane, or icono floor models are most at risk. Patients and staff could be injured if the table detaches during procedures.
Check for the specific material numbers: 10849000 for ARTIS pheno, 11327600 for icono biplane, and 11327700 for icono floor. Also look for the UDI/DI numbers listed in the recall notice.
Inspect the mechanical connection between the tabletop and table base for signs of looseness or damage.
Reach out to Siemens Medical Solutions USA, Inc for guidance on repair or replacement options.
The ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor models are affected.
Check for the material numbers: 10849000 for ARTIS pheno, 11327600 for icono biplane, and 11327700 for icono floor. Also look for the UDI/DI numbers listed in the recall notice.
Inspect the connection for looseness or damage and contact Siemens Medical Solutions USA, Inc for repair or replacement options.
We’ve drafted a message you can send Siemens Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0956-2023 — Siemens Medical Siemens Medical Hello, I own a Siemens Medical that is covered by recall Z-0956-2023 from Siemens Medical. 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.
