Mahurkar Acute Dual Lumen Catheter Kits
Brand(s)
Last updated
Summary
Product
Mahurkar Acute Dual Lumen Catheter Kits
Issue
Medical devices - Performance
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 and 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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