Tag: Medtronic

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Customers are being asked to remove the affected devices from use and replace with an alternate means of ventilation.

Medtronic has received the European CE Mark approval for its Inceptiv closed-loop rechargeable spinal cord stimulator (SCS).

Medtronic received U.S. FDA approval for expanded labeling of a cardiac lead that taps into the heart's natural electrical system.

Customers are being asked to remove the affected devices from use and replace with an alternate means of ventilation.

Aug 22, 2022

Medtronic is recalling Cobalt/Crome implantable cardioverter defibrillators and cardiac resynchronization therapy defibrillators.

Jul 18, 2022

The algorithm leverages machine learning to help surgeons plan and personalize procedures for patients undergoing lower lumbar spine surgery.

Jun 27, 2022

Amid continued recall concerns, devices from Medtronic and Baxter were recently assigned the most serious recall type be the FDA.

Jun 9, 2022

Medtronic recalled its HeartWare Ventricular Assist Device System, which is designed to help the heart pump blood to the rest of the body.

May 26, 2022

Medtronic and DaVita intend to form a kidney care medical device company to enhance the patient treatment experience.

May 3, 2022

The Medtronic Heartware Ventricular Assist Device (HVAD) System may have a welding defect in the internal pump causing a malfunction.

Covidien, LP is recalling its Puritan Bennett 980 Series Ventilator due to a capacitor manufacturing assembly error.