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

Medtronic Recalls Evera, Viva, Brava, Claria

2021年4月12日—MedtronicRecallsEvera,Viva,Brava,Claria,Amplia,Compia,andVisiaImplantableCardioverterDefibrillators(ICDs)andCardiac ...

 Medtronic Recalls Evera, Viva, Brava, Claria

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

Recalled Product Medtronic Evera, Viva, Brava, Claria, Amplia, Compia, and Visia Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy (CRT-Ds) Models: Full List of Affected Devices below Serial Numbers: Full List of Affected Devices below Distribution Dates: August 31, 2012 to May 9, 2018 Devices Recalled in the U.S.: 239,171 Date Initiated by Firm: February 3, 2021 Device Use

Medtronic’s Evera, Viva, Brava, Claria, Amplia, Compia, and Visia Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy (CRT-Ds) are devices that provide pacing for slow heart rhythms, and electrical shock or...

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FDA | 合法醫療器材資訊網
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
Medtronic Recalls Evera, Viva, Brava, Claria | 合法醫療器材資訊網
2021年4月12日 — Medtronic Recalls Evera, Viva, Brava, Claria, Amplia, Compia, and Visia Implantable Cardioverter Defibrillators (ICDs) and Cardiac ... Read More
2020 Medical Device Recalls | 合法醫療器材資訊網
List of Medical Device recalls in 2020. ... Separate During Use, 11/09/20. Medtronic Recalls Rashkind Balloon Septostomy Catheters for Quality Issues, 11/​03/20. Read More
Medtronic | 合法醫療器材資訊網
2019年2月15日 — Reason for Recall. Medtronic is recalling its dual chamber IPGs due to the possibility of a software error that can result in a lack of pacing. Patients ... Read More
2021 Medical Device Recalls | 合法醫療器材資訊網
List of Medical Device recalls in 2021. ... 2021 Medical Device Recalls · 2020 Medical Device Recalls · 2019 Medical Device Recalls · 2018 ... Abbott (formally known as St. Jude Medical) Recalls Assurity™ and Endurity™ Pacemakers for ... Medtronic, Inc. R Read More
Medtronic Recalls its ICDs and CRT | 合法醫療器材資訊網
2021年4月12日 — Medtronic Recalls its ICDs and CRT-Ds Due to Risk of Rapid Battery Depletion ... Medtronic is recalling some of its implantable cardioverter ... Read More
Dual Chamber Pacemakers | 合法醫療器材資訊網
2019年1月7日 — Through 4 January 2019, Medtronic is aware of four (4) reported occurrences in two (2) patients where a pause in pacing therapy was clinically ... Read More
Medical Device Recalls | 合法醫療器材資訊網
Results 1 - 9 of 9 — Z-2507-2020 - Azure XT DR MRI, Model Numbers: a) W1DR01 and b) W2DR01​17, 2, 07/10/2020, Medtronic Inc., Cardiac Rhythm and Heart ... Read More
FDA delayed reporting | 合法醫療器材資訊網
2020年2月12日 — Medtronic and the FDA were both aware of battery and wire connection defects in a now-recalled heart failure pacemaker for over a year before ... Read More
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