Medtronic's Entrust Dual Chamber (2018-06-21)

Medtronic EnTrust Dual Chamber Recall Summary Medtronic is recalling EnTrust Dual Chamber devices across Canada due to a medical device issue. The devices are implantable cardiac devices used to regulate heart rhythm. The recall affects all units distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-07-05
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ff706a04-e6d9-4d0b-9238-877aca4c0ad3