Siemens recalls Artis zee floor interventional fluoroscopy systems with specific model numbers due to potential screw failure that could cause severe injuries to patients and staff during procedures.
Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel
Siemens is recalling certain Artis zee floor interventional fluoroscopy systems because screws connecting the pivot bearing to the ceiling support may become loose or snap, risking serious injuries to patients and medical staff. This recall affects specific model numbers and serials listed in the notice.
The system's screws that join the pivot bearing to the ceiling support may work loose or snap during use. This can cause the equipment to become unstable, potentially leading to falls or injuries for patients and medical staff during procedures.
Medical facilities using the recalled Artis zee floor interventional fluoroscopy systems with specific model numbers and serials are most at risk. Patients and operating personnel during procedures could face severe injuries if the system fails.
Check if your system has model number 10094135 and the listed serial numbers (e.g., 135954, 136032, etc.). The recall applies to specific Artis zee floor interventional fluoroscopy systems sold with DCS Extended or DCS Movable configurations.
Discontinue use of the recalled Artis zee floor interventional fluoroscopy system to prevent potential screw failure causing injuries.
Model number 10094135 with specific serial numbers listed in the recall notice.
The screws connecting the pivot bearing to the ceiling support may become loose or snap, risking severe injuries to patients and medical staff during procedures.
Check if your system has model number 10094135 and one of the listed serial numbers (e.g., 135954, 136032, etc.).
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1894-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1894-2019 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.
