Siemens recalls Artis Zee ceiling fluoroscopy systems with model 10094137 and specific serial numbers due to potential screw failure causing severe injuries during medical 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 Artis Zee ceiling fluoroscopy systems with model number 10094137 that could have screws loosening or snapping, risking serious injury to patients and medical staff. This recall affects specific serial numbers listed in the official notice.
The system's pivot bearing connection to the ceiling support uses screws that may work loose or snap during operation. This could cause the system to become unstable, potentially leading to falls or injuries for patients and medical staff.
Healthcare facilities using the Artis Zee system with model 10094137 and the listed serial numbers are most at risk. Patients and medical personnel during procedures could face severe injuries if the system malfunctions.
Check if your Siemens Artis Zee system has model number 10094137 and the specific serial numbers listed in the recall notice. The system is used in medical settings for interventional fluoroscopy procedures.
Discontinue use of the Artis Zee system with model 10094137 and the listed serial numbers to prevent potential injury.
Model number 10094137 with specific serial numbers listed in the recall notice.
Check if your Siemens Artis Zee system has model number 10094137 and one of the serial numbers provided in the recall notice.
The recall notice does not specify a remedy; users must stop using the affected systems immediately.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1895-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1895-2019 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.
