Product Wiki · Recalls · Health Canada — Medical Devices

High Flow Insufflation Tubing (With Filter) — recall 75923

Health Canada — Medical Devices · Canada · 2024-08-15 · 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
75923
Date of alert
2024-08-15
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Obstetrics and gynaecology
Product type
Medical devices
Reported risk: The unit package seal failed and it compromised sterility. Although one defect was detected in the field, no adverse events have occurred as a result of this incident. Inspection of inventory on-hand determined that there may be around 1% of this product (p/n 20400161S, lot #185198) with opened seals and if used could result in patient infections. Recall Start Date: July 19, 2024
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/high-flow-insufflation-tubing-

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.