Product Wiki · Recalls · Health Canada — Medical Devices

Signa MR Systems — recall 75806

Health Canada — Medical Devices · Canada · 2026-07-28 · 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 on this page. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
75806
Date of alert
2026-07-28
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: B1+RMS predicted value may exceed user prescribed limit in low SAR mode for certain MR systems. Recall start date: June 14, 2024
What to do

Check whether your product matches this notice (name, batch, dates). If it does, stop using it and follow the instructions in the official notice — refund, return, repair or disposal are set by the issuing authority and the business, and they differ per recall. Official notice from Health Canada — Medical Devices →

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/signa-mr-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.