Siemens recalls Artis Q ceiling X-ray systems with specific serial numbers due to potential screw failure that could cause 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 Q ceiling X-ray systems because screws connecting the machine to the ceiling could become loose or snap, risking serious injuries to patients and medical staff. This is a critical safety issue that requires immediate attention.
The screws that attach the X-ray system to the ceiling can become loose or break during use. This could cause the machine to fall or move unexpectedly, potentially injuring patients and medical staff during critical procedures.
Healthcare facilities using the recalled Siemens Artis Q X-ray systems with the listed serial numbers are most at risk. Medical personnel and patients during procedures could be injured if the system malfunctions.
Check if your Siemens Artis Q X-ray system has a serial number listed in the provided list (e.g., 109007, 109057, etc.). The system model is identified as Artis Q with specific DCS Extended or DCS Movable configurations.
Immediately cease using the recalled Siemens Artis Q X-ray system if it has a serial number from the provided list.
The affected models are Siemens Artis Q ceiling X-ray systems with serial numbers listed in the provided list (e.g., 109007, 109057, etc.).
Check your system's serial number against the list of numbers provided in the recall notice. The list includes specific serial numbers like 109007, 109057, and others.
Immediately stop using the system and contact Siemens for further instructions. The recall requires immediate action to prevent potential injury.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1899-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1899-2019 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.
