Brand Recall Hub

Medtronic Recalls in Canada

14 recalls found for Medtronic. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

14 Medtronic Recalls

Medical Devices Type II
2025-11-28

Medtronic Restore™ Clinician Programmer Application

Performance

View recall details →
Medical Devices Type II
2024-12-19

Medtronic Fixator Pins - Stainless Steel

Device compatibility

View recall details →
Medical Devices Type II
2024-07-25

Medtronic XPS System - Burs

Sterility

View recall details →
Medical Devices Type II
2024-04-03

Medtronic Cannulae Products

Sterility

View recall details →
Medical Devices Type I
2023-05-25

Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds)

Performance

View recall details →
Medical Devices Type I
2022-12-13

Medtronic Nonabsorbable Sutures

Sterility

View recall details →
Medical Devices Type II
2022-02-08

Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console (2021-03-05)

Manufacturing defect

View recall details →
Medical Devices Type II
2021-08-27

Medtronic HeartWare Ventricular Assist Device (HVAD) System/licence (2021-08-11)

Medical devices

View recall details →
Other
2021-06-25

Medtronic Heartware Ventricular Assist Device System - Recall Due to Risk of Neurological Adverse Events, Mortality and Delay or Failure to Restart

Medical devices - Product safety

View recall details →
Other
2019-06-29

Certain older Medtronic MiniMed insulin pumps may be vulnerable to cybersecurity risks

View recall details →
Medical Devices Type II
2019-02-22

Medtronic Stent Graft Systems (2019-02-10)

Medical devices

View recall details →
Medical Devices Type II
2019-02-08

Medtronic Programmers (CareLink, Encore), Medtronic Micra (2019-01-16)

Medical devices

View recall details →
Medical Devices Type I
2019-01-30

Medtronic Adapta Pacing System (Adapta, Sensia, Attesta) (2019-01-14)

Medical devices

View recall details →
Medical Devices Type I
2018-07-05

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

Medical devices

View recall details →