Product Wiki · Recalls · Health Canada — Medical Devices

CENTRY SYSTEM HEMODIALYSIS BLOOD TUBING SET AND CARTRIDGE (2021-01-05) — recall 62007

Health Canada — Medical Devices · Canada · 2021-01-15 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
62007
Date of alert
2021-01-15
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Baxter Corporation has received customer reports of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/centry-system-hemodialysis-blo

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