Siemens recalls Artis Q biplane 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 biplane X-ray systems because screws connecting the machine to the ceiling could become loose or snap, risking serious injury to patients and 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 work loose or snap during use. This could cause the X-ray machine to move unexpectedly, potentially leading to falls, lacerations, or other serious injuries for both patients and medical staff.
Healthcare facilities using the recalled Artis Q biplane X-ray systems with specific serial numbers are at risk. Medical personnel and patients undergoing procedures with these systems could face severe injuries if the screws fail.
Check if your Siemens Artis Q biplane X-ray system has the model number 10848282 and the listed serial numbers (e.g., 121013, 121057, etc.). The recall applies to specific systems used in medical facilities.
Discontinue use of the recalled Artis Q biplane X-ray system until a replacement is installed or the issue is resolved.
The affected model is 10848282 with specific serial numbers listed in the recall notice.
Check if your Siemens Artis Q biplane X-ray system has the model number 10848282 and the listed serial numbers (e.g., 121013, 121057, etc.).
Contact Siemens Medical Solutions USA, Inc. directly to arrange for a replacement or repair of the affected system.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1900-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1900-2019 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.
