Product Wiki · Recalls · Health Canada — Medical Devices

Curver Reinforced Endotracheal Tube — recall 52666

Health Canada — Medical Devices · Canada · 2015-01-28 · Type III

As described by Health Canada — Medical Devices: Curver Reinforced Endotracheal Tube - Murphy Eye, High Volume, Low Pressue Cuff - Sterile Pack (2013-12-30)

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
52666
Date of alert
2015-01-28
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Teleflex Medical is issuing an advisory notification to customers who have received the affected products because of an awareness of a minimal discrepancy between the labeled cuff diameter and the actual cuff diameter of the endotracheal tube.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/curver-reinforced-endotracheal

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.