Product Wiki · Recalls · Health Canada — Medical Devices

Percutaneous Sheath Introducer Kits with Silk Sutures (2014-05-01) — recall 51330

Health Canada — Medical Devices · Canada · 2014-05-08 · 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
51330
Date of alert
2014-05-08
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: Arrow is recalling the products referenced above due to dilator tip damage noted during internal inspection of the percutaneous sheath introducer kits. Dilator tip damage has the potential to result in vessel damage. There are no reported related illnesses or injuries from the related device.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/percutaneous-sheath-introducer

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.