Product Wiki · Recalls · Health Canada — Medical Devices

Neonatal-Infant and Adult Pediatric Filter and Sampling Lines — recall 77069

Health Canada — Medical Devices · Canada · 2025-03-06 · 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: 77069
Date of alert: 2025-03-06
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Anaesthesiology
Product type: Medical devices

Reported risk: Medtronic is issuing an update to Instruction For Use (IFU) following reports of difficulty or inability in disconnecting the adapter from patient's endotracheal tube to perform a procedure. As noted in the IFU, during setup, ensure that the airway adapter can be easily attached and detached from the breathing circuit/tubing before proceeding. Recall Start Date: February 19, 2025

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/neonatal-infant-and-adult-pedi

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.

Neonatal-Infant and Adult Pediatric Filter and Sampling Lines — recall 77069

Related