Health Canada — Medical Devices · Canada · 2025-05-15 · 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 →
Reported risk: Cardinal Health has initiated a medical device product recall on specific product codes and lots of Umbilical Vessel Catheters. The list of affected product codes and lots are being recalled due to a possible packaging defect impacting the outer tyvek pouch that protects the sterile product. This pouch is used on both the Single-Sterile Umbilical Vessel Catheters and the product within a finished insertion tray. This defect may allow for small holes to develop in the pouch which could potentially compromise the sterility of the product. These holes may be undetectable upon visual inspection, so none of the identified lots should be used. Recall Start Date: May 5, 2025
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.