Product Wiki · Recalls · Health Canada — Medical Devices

Rusch Bronchopart and Rusch Bronchopart White Bronchial Tubes… — recall 51334

Health Canada — Medical Devices · Canada · 2014-03-04 · Type II

As described by Health Canada — Medical Devices: Rusch Bronchopart and Rusch Bronchopart White Bronchial Tubes (2014-03-04)

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
51334
Date of alert
2014-03-04
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: The products may fail to achieve seal of right lung due to the cuff inflating to one side. If a seal does not occur there is the potential for oxygen de-saturation and loss of volatile anesthetics, requiring re-intubation of the patient.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/rusch-bronchopart-and-rusch-br

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.