Product Wiki · Recalls · Health Canada — Medical Devices

MOSAIQ — recall 76878

Health Canada — Medical Devices · Canada · 2025-01-29 · 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
76878
Date of alert
2025-01-29
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: MOSAIQ 2D image review application may provide incorrect image offsets when a 2D verification image is taken at a patient support angle (couch rotation) other than 0 degrees, and if the treatment machine is characterized at a scale that is not IEC61217. If the incorrect shift was not detected and used for treatment, mistreatment could occur. Recall start date: January 15, 2025
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/mosaiq-1

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.

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.