Centry System Hemodialysis Blood Tubing Set And Cartridge (2021-01-05)

Recall Summary Centry System hemodialysis blood tubing sets and cartridges are being recalled in Canada due to a medical device issue. This recall affects hemodialysis patients who use this equipment for kidney treatment. The recall is classified as Class I, indicating a serious potential health concern.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-01-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1fad8bbd-9ff2-41eb-88c8-c1a819293244