Artiset Blood Tubing Set for Haemodialysis - HD DNL HC (2021-04-29)

Starting date:

April 29, 2021

Posting date:

May 6, 2021

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-75535

Last updated:
2021-05-06

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  Reason
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  Affected products

Affected Products 

Artiset Blood Tubing Set for Haemodialysis - HD DNL HC

Reason

Baxter Corporation is issuing a voluntary product recall to users for one lot of Hemodialysis Cartridge  Blood Sets due to customer reports of external leak events between the venous patient connector and the hemodialysis (HD) access caused by damage on the male portion of venous connector.

Affected products