Siemens recalls Artis Zee X-Ray systems with model 10094141 and specific serial numbers due to risk of screws loosening, potentially 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 certain Artis Zee X-ray systems that could have loose or broken screws, which might cause serious injuries to patients or medical staff during procedures. This recall affects specific models and serial numbers.
Screws connecting the pivot bearing to the ceiling support may work loose or snap off during use. This could cause the X-ray system to become unstable, leading to falls or injuries for patients and medical staff.
Medical facilities using the recalled Artis Zee X-ray systems with model number 10094141 and listed serial numbers are most at risk. Patients and medical personnel during procedures could be injured if the system malfunctions.
Check if your Siemens Artis Zee X-ray system has model number 10094141 and one of the listed serial numbers (e.g., 153883, 154041, etc.).
Immediately stop using the affected Siemens Artis Zee X-ray system if it has model number 10094141 and one of the listed serial numbers.
Model number 10094141 with serial numbers including 153883, 154041, 153640, and others listed in the recall notice.
The recall is due to a risk that screws connecting the pivot bearing to the ceiling support could loosen or snap off, potentially causing severe injuries during medical procedures.
No action is needed if your Siemens Artis Zee X-ray system does not have model number 10094141 or the listed serial numbers.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1896-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1896-2019 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.
