Health Canada — Medical Devices · Canada · 2025-11-10 · 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 →
Reported risk: The action is being initiated due to a potential issue with the smoothbore hoses of the catheter mounts. Under stress, these hoses could tear, potentially resulting in leakage. If leakage occurs, the ability of ventilators or anesthesia devices to compensate depends on the size of the leak and the ventilation pressure settings. In cases where compensation is not possible, ventilation may be restricted, posing a risk of desaturation or hypoxia for the patient.
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.