Product Wiki · Recalls · Health Canada — Medical Devices

MAGNETOM Sola (2020-02-27) — recall 63236

Health Canada — Medical Devices · Canada · 2020-03-13 · Type III

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
63236
Date of alert
2020-03-13
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: The software update to NX VA20A resolves the following issues and prevents them from recurring. The update is not providing new features or new functionality. These fixes do not affect patient safety. Several improvements for PACS export Various Dicom tag and image text corrections Table position using select & go autopositioning corrected Image quality using save-as-series improved Prior study handling improved Orientation of composed spine images corrected General stability & performance improvements in: Patient registration Workflow configuration and execution System boot and shutdown
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/magnetom-sola-2020-02-27

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.