No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
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An official Health Canada notice concerns Mahurkar acute dual lumen catheter kits. 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 Published 2022-12-22.
What to do now
Contact the manufacturer if you require additional information.
Recall number
72401
Official notice
2022-12-22
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Turn on recall alertsAffected products
Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Covidien, Mahurkar Acute Dual Lumen Catheter Kits.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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