Siemens recalls Artis Q floor, ceiling, and biplane X-ray systems with specific model numbers due to a potential error detection issue that may prevent X-ray release in rare cases.
Siemens has become aware of a potential hardware issue with Artis Q, Artis Q.zen, Artis pheno and Artis icono systems with a specific lot of X-ray tubes. In rare cases, if the error detection mechanism fails, it will not be possible to release X-ray any longer until system shutdown.
Siemens is recalling Artis Q X-ray systems (floor, ceiling, and biplane models) with specific model numbers because a hardware issue could cause the system to stop releasing X-rays in rare cases if the error detection mechanism fails. This could lead to interrupted imaging procedures.
The recall involves a potential hardware issue with the X-ray tube error detection mechanism. In rare cases, if this mechanism fails, the system may not be able to release X-ray images until it shuts down, interrupting imaging procedures.
Medical facilities using Siemens Artis Q X-ray systems with the listed model numbers are affected. Patients undergoing X-ray procedures may be impacted if the system stops functioning during a scan.
Check for the model numbers listed in the recall (e.g., Artis Q floor Model No. 10848280, ceiling Model No. 10848281, biplane Model No. 10848282) and serial numbers provided in the recall notice.
Verify your Artis Q system's model number against the list of affected models provided in the recall notice.
Siemens has identified a potential hardware issue with the error detection mechanism in specific X-ray tubes that could cause the system to stop releasing X-rays in rare cases if the error detection fails.
No. The recall does not require immediate discontinuation of use. The hazard is rare and only affects specific model numbers.
Check your Artis Q system's model number and serial numbers against the list provided in the recall notice.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1645-2022 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1645-2022 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.
