Product Wiki · Recalls · Health Canada — Medical Devices

Ruby Set V2 Tubing (2014-12-19) — recall 53005

Health Canada — Medical Devices · Canada · 2014-12-30 · Type III

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
53005
Date of alert
2014-12-30
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: Some specific lots of the Ruby Set V2 Tubing may potentially leak during patient treatment.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/ruby-set-v2-tubing-2014-12-19

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.