Product Wiki · Recalls · Health Canada — Medical Devices

Embol-X Arterial Cannula and Embol-X Kit, Glide Cannula with Suture… — recall 50118

Health Canada — Medical Devices · Canada · 2013-10-31 · Type II

As described by Health Canada — Medical Devices: Embol-X Arterial Cannula and Embol-X Kit, Glide Cannula with Suture Flange and Filter (2013-10-02)

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
50118
Date of alert
2013-10-31
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Potential health risk to patients undergoing cardio pulmonary by-pass surgery when using the Embol-X Glide Protection system. The tip of the cannula may be deformed. If the defect is not noticed during preparation, when force is applied to the tip during insertion or removal, it may lead to a separation and embolize.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/embol-x-arterial-cannula-and-e

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.