Health product recall

Mahurkar Acute Dual Lumen Catheter Kits

Brand(s)
Last updated

Summary

Product
Mahurkar Acute Dual Lumen Catheter Kits
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
Mahurkar Acute Dual Lumen Catheter Kits More than 10 numbers, contact manufacturer. 8888135161 8888135162 8888135192 8888135133 8888135241 8888135242 8888135191

Issue

During the production process, a potential internal leaking condition within the hub of specific Mahurkar acute dual lumen high flow  hemodialysis catheter was identified as a result of a void in the catheter hub. During dialysis, this observed adverse internal leaking condition could translate into cross communication of the blood circuit.

Recall start date: December 7, 2022

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Gastroenterology & Urology
Companies

Covidien Llc

15 Hampshire Street, Mansfield, Massachusetts, United States, 02048

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-72401

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