Product Wiki · Recalls · Health Canada — Medical Devices

Raystation — recall 75202

Health Canada — Medical Devices · Canada · 2024-03-08 · 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
75202
Date of alert
2024-03-08
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: This recall concerns a use error that has occurred with Raystation, where material override using silicon, SI, was incorrectly selected for a silicone gel polymer implant. Recall start date: February 23, 2024
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/raystation-2

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.