Home/Recalls/CANADA-60837
Health CanadaGeneral Alert

Percutaneous Radiofrequency Ablation Catheter and the Potential Risk of Atrioeso...

Published: April 16, 2018Recall ID: 60837Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Percutaneous Radiofrequency Ablation Catheter and the Potential Risk of Atrioesophageal Fistula

Additional Source Details

FieldValue
N I D60837
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/percutaneous-radiofrequency-ablation-catheter-and-potential-risk-atrioesophageal
IssueMedical devices
Title Percutaneous Radiofrequency Ablation Catheter and the Potential Risk of Atrioesophageal Fistula
Archived0
CategoryMedical devices
Last updated2018-04-16
OrganizationMarketed health products

Overview

  • Recalling FirmMarketed health products
Official Agency Alert