FDA delayed reporting | 合法醫療器材資訊網

2020年2月12日—MedtronicandtheFDAwerebothawareofbatteryandwireconnectiondefectsinanow-recalledheartfailurepacemakerforoverayearbefore ...

After graduating from Indiana University-Bloomington with a bachelor’s in journalism, Anicka joined TriMed’s Chicago team in 2017 covering cardiology. Close to her heart is long-form journalism, Pilot G-2 pens, dark chocolate and her dog Harper Lee.

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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) W2DR0117, 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

相關資訊整理

FDA delayed reporting | 合法醫療器材資訊網

FDA | 合法醫療器材資訊網

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

2020 Medical Device Recalls | 合法醫療器材資訊網

Medtronic | 合法醫療器材資訊網

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

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

Dual Chamber Pacemakers | 合法醫療器材資訊網

Medical Device Recalls | 合法醫療器材資訊網

FDA delayed reporting | 合法醫療器材資訊網

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