Product Wiki · Recalls · Health Canada — Medical Devices

Artis Q and Zee Systems — recall 72506

Health Canada — Medical Devices · Canada · 2023-01-03 · Type II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
72506
Date of alert
2023-01-03
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: In rare cases, the system may only boot into backup mode after an abrupt shutdown and not reach full operating mode. The full system functionality is not available. Only the backup mode is available, as mentioned in the operator manual. The Syngo start-up screen on the monitor of the system console in the control room does not disappear, which causes a never-ending count on the monitor. Recall start date: December 20, 2022
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/artis-q-and-zee-systems

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.