Siemens recalls Artis Q zeego Interventional Fluoroscopic X-Ray System (model 10848283) due to risk of screws loosening or snapping, 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 its Artis Q zeego Interventional Fluoroscopic X-Ray System (model 10848283) because screws connecting the pivot bearing to the ceiling support could loosen or snap, risking serious injury to patients and medical staff. This is a critical safety issue that requires immediate attention to prevent harm.
The system's screws that connect the pivot bearing to the ceiling support can become loose or snap during use. This could cause the equipment to malfunction, potentially leading to severe injuries for patients and medical staff during procedures.
Healthcare facilities using the Siemens Artis Q zeego system with model number 10848283 are affected. Medical personnel and patients undergoing procedures on these systems are at highest risk.
Check for the model number 10848283 on the Siemens Artis Q zeego system. The serial numbers 117309 and 117125 are also associated with this recall.
Immediately cease using the Siemens Artis Q zeego Interventional Fluoroscopic X-Ray System with model number 10848283 to prevent potential injury.
The model number is 10848283.
The serial numbers 117309 and 117125 are affected.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1901-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1901-2019 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.
