Medtronic Recalls its ICDs and CRT | 合法醫療器材資訊網

April12,2021—Medtronicisrecallingsomeofitsimplantablecardioverterdefibrillators(ICD)andcardiacresynchronizationtherapy(CRT-D)devicesbecause ...

April 12, 2021 — Medtronic is recalling some of its implantable cardioverter defibrillators (ICD)[1] and cardiac resynchronization therapy (CRT-D)[2] devices because of an unexpected and rapid decrease in battery life. The company said this is due to a short circuit and will cause some devices to produce a “Recommended Replacement Time” (first warning that the battery is low) earlier than expected. Some devices may progress from “Recommended Replacement Time” to full battery depletion within as little as one day.

If the user does not respond to the first warning, the device may stop functioning, Medtronic said. The likelihood that this issue will occur is constant after approximately three years. after device use.

The U.S. Food and Drug Administration (FDA) issued a a notice April 12 that identified this as a class I recall, the most serious type of recall. Use of these devices may caus...

Medtronic Recalls its ICDs and CRT | 合法醫療器材資訊網

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

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

沒有這個頁面的資訊。 Read More

2021 Medical Device Recalls | 合法醫療器材資訊網

Medtronic Recalls Evera, Viva, Brava, Claria, Amplia, Compia, and Visia Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy ... Read More

Medtronic Recalls Evera, Viva, Brava, Claria | 合法醫療器材資訊網

2021年4月12日 — Reason for Recall ... Medtronic is recalling the specified ICDs and CRT-Ds due to an unexpected and rapid decrease in battery life. The decrease ... Read More

FDA | 合法醫療器材資訊網

2021年4月12日 — Medtronic issued an urgent medical device correction letter to healthcare providers on February 3, 2021, advising them to continue normal ... Read More

FDA details Class I recall of nearly 240 | 合法醫療器材資訊網

2021年4月15日 — Medtronic first initiated the recall, which includes a total of 239,171 devices, in February 2021. All affected healthcare providers were alerted at ... Read More

Implantable Cardioverter Defibrillator (2021-02 | 合法醫療器材資訊網

2021年2月19日 — Medtronic Inc. 710 Medtronic Parkway Minneapolis 55432. Minnesota UNITED STATES. E. EVERA XT DR DIGITAL DUAL CHAMBER ... Read More

FDA classifies Medtronic ICD | 合法醫療器材資訊網

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

https:global.medtronic.comxg | 合法醫療器材資訊網

沒有這個頁面的資訊。 Read More

Medtronic has a serious recall of ICDs and CRT | 合法醫療器材資訊網

2021年4月12日 — FDA has issued a Class I designation of a Medtronic (NYSE: MDT) recall involving 239,171 ICDs and CRT-Ds with potential battery life ... Read More

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