Medtronic recalls nearly 157,000 dual-chamber pacemakers - OR Manager
Warnings for varenicline, bupropion; pacemaker recalled | ACP Internist
Medtronic snags another Class I recall, this time for its artery-clearing HawkOne system | Fierce Biotech
Follow-up After Pacemaker Implantation | SpringerLink
Urgent Field Safety Notice
Perioperative Interrogation of Medtronic Cardiovascular Implantable Electronic Devices: A Guide for Anesthesiologists
Cardiac Rhythm Heart Failure
FDA Issues Class 1 Recall for Over 150K Medtronic Pacemakers
FDA announces recall of nearly 88,000 implantable cardiac devices due to risk of serious injury or death
April 05
CRM PRODUCT PERFORMANCE REPORT
Pacemakers found to be seriously vulnerable to hacking - SiliconANGLE
FDA approves first and only MRI-safe pacemaker - CNET
Cardiac Rhythm Device Identification Algorithm using X-Rays: CaRDIA-X - ScienceDirect
Perioperative Interrogation of Medtronic Cardiovascular Implantable Electronic Devices: A Guide for Anesthesiologists
A Defective Pacemaker Can Cause More Harm Than Good
FDA Calls Class I Recall on Some Medtronic Kappa, Sigma Pacemakers | DAIC
FDA Calls Class I Recall on Some Medtronic Kappa, Sigma Pacemakers | DAIC
PDF) Design of the Pacemaker REmote Follow-up Evaluation and Review (PREFER) trial to assess the clinical value of the remote pacemaker interrogation in the management of pacemaker patients
Noise Rejection Feature in Boston Scientific Pacemakers
Medtronic Cardiac Defibrillators Recalled Due To Plant Problem - The Eichholz Law Firm
