Siemens recalls Artis Q floor-based interventional fluoroscopy systems with model 10848280 due to potential loose or snapped screws causing severe injuries during use. Affected units include specific serial numbers listed in the recall notice.
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 Q floor-based interventional fluoroscopy systems because screws connecting the pivot bearing to the ceiling support could become loose or snap off, risking severe injuries to patients and staff. This recall affects specific model and serial numbers listed in the notice.
The system's screws that join the pivot bearing to the ceiling support may work loose or snap off during use. This can cause the equipment to become unstable, leading to falls or injuries for both patients and medical personnel.
Healthcare facilities using the recalled Siemens Artis Q systems with model number 10848280 and listed serial numbers are most at risk. Patients and medical staff during procedures using these systems could face serious injuries.
Check for the model number 10848280 on the system. Affected units have specific serial numbers listed in the recall notice: 103008, 103030, 103028, 103258, 103221, 103222, 103277, 103220, 103279, 103285, 103286, 103295.
Immediately stop using the recalled Siemens Artis Q floor-based interventional fluoroscopy system with model number 10848280 and listed serial numbers to prevent potential injuries.
The affected model number is 10848280.
Affected serial numbers include 103008, 103030, 103028, 103258, 103221, 103222, 103277, 103220, 103279, 103285, 103286, 103295.
The recall notice does not specify a remedy; affected users must stop using the system immediately.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1898-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1898-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
