Urgent Medical Device Correction | 合法醫療器材資訊網

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Medtronic Vascular Recalls Angiographic Guidewire Component Due to Being ... Compia, and Visia Implantable Cardioverter Defibrillators (ICDs) and Cardiac ... Read More

Medtronic is recalling some of its implantable cardioverter defibrillators (ICD) and cardiac resynchronization therapy. April 12, 2021 — Medtronic is recalling ... Read More

2021年4月12日 — The devices are being recalled due to an unexpected and rapid decrease in battery life caused by a short circuit. This defect may case some ... Read More

On March 16, 2018- Medtronic announced a voluntary recall affecting 752 Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) and Implantable ... Read More

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2021年4月12日 — The US Food and Drug Administration has declared Medtronic's recall of seven models of defibrillating cardiac rhythm devices, due to a risk for ... Read More

2021年4月12日 — According to a press release from the agency, Medtronic recalled its Evera and Visia brands of ICDs and its Viva, Brava, Claria, Amplia and ... Read More

2021年4月15日 — Devices impacted by the recall include Medtronic's Evera, Viva, Brava, Claria, Amplia, Complia and Visia ICDs and CRT-Ds. The battery issue is ... Read More

The defects found in the Medtronic pacemaker and defibrillator models were discovered to cause an “out of specification gas mixture inside the device which may ... Read More