Minimed Mio Advance (2018-12-18)

MiniMed Mio Advance Recall Summary Medtronic is recalling MiniMed Mio Advance infusion sets across Canada because the devices may disconnect or detach from insulin pumps, potentially interrupting insulin delivery to patients who depend on them. This is classified as a Class I recall, meaning there is a serious risk of adverse health effects. The recall affects all MiniMed Mio Advance infusion sets distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-01-11
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f1bd5389-8949-414c-b719-b0108044abab