台中港酒店親子飯店開箱+５大親子主題房

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

2020 Medical Device Recalls

ListofMedicalDevicerecallsin2020....SeparateDuringUse,11/09/20.MedtronicRecallsRashkindBalloonSeptostomyCathetersforQualityIssues,11/​03/20.

 2020 Medical Device Recalls

We’re sorry. The page you are looking for is not available for one of the following reasons.

The link to this page may not be correct or is out-of-date. You have bookmarked a page that has moved.

Try one of these options:

Search FDA.gov Check the FDA Archive Contact FDA[1][2][3]

Or try one of these helpful links to FDA topics:

References Search FDA.gov (www.fda.gov) Check the FDA Archive (www.fda.gov) Contact FDA (www.fda.gov)

閱讀更多

medtronic defibrillator medtronic defibrillator recall abbott pacemaker recall 2021 defibrillator recall 2020 medtronic recall list fda medical device recalls 2020 fda medtronic pacemaker recall medtronic pacemaker recall lawsuit Abbott pacemaker medtronic pacemaker recall 2020 Medtronic pacemaker abbott pacemaker model pm2272 boston scientific pacemaker recall Medtronic recall 2021 abbott pacemaker monitor recall governor abbott fda medical device recalls 2021 FDA medical device Recall 2020 FDA recall Medical device Medical device safety FDA recall classification FDA CDRH medtronic icd price medtronic pacemaker Implantable cardioverter defibrillator Medtronic CRHF Medtronic ICD medtronic icd price in india medtronic icd models medtronic defibrillator pacemaker defibrillator recall 2020 medtronic recall lookup abbott pacemaker recall 2021 medtronic recall list medtronic fibercel recall medtronic recall 2020 medtronic defibrillator manual medtronic recall hvad medtronic pacemaker recall medtronic pacemaker recall 2021 腦 波 膠 eg med口罩 NIPRO APPALEAD HYDROPHILIC GUIDE WIRE "PIOLAX" 東 耀 尿酮試紙 "和德" 血小板貯存容器 (未滅菌) “邁瑞”中央監視系統 "BD"抗生素感受性試驗紙錠-合成青黴素類 “Boditech” Hemochroma PLUS
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
相關資訊整理

【“美敦力”艾坦冠狀動脈竇導管】許可證字號:衛署醫器輸字第009197號

器材品名:“美敦力”艾坦冠狀動脈竇導管許可證字號:衛署醫器輸字第009197號註銷狀態:已註銷註銷日期:2016/11/15註銷理由:未展...

【自體輸血系統】許可證字號:衛署醫器輸字第008366號

器材品名:自體輸血系統許可證字號:衛署醫器輸字第008366號註銷狀態:已註銷註銷日期:2005/04/13註銷理由:未展延而逾期者有效...

【“美敦力”胸主動脈支架系統】許可證字號:衛署醫器輸字第020704號

器材品名:“美敦力”胸主動脈支架系統許可證字號:衛署醫器輸字第020704號註銷狀態:已註銷註銷日期:2018/04/25註銷理由:許可證...

【"美敦力" 抽吸/抗凝血套組】許可證字號:衛署醫器輸字第010069號

器材品名:"美敦力"抽吸/抗凝血套組許可證字號:衛署醫器輸字第010069號註銷狀態:註銷日期:註銷理由:有效日期:2022/09/10發證...

【艾維血管擴張氣球導管】許可證字號:衛署醫器輸字第020573號

器材品名:艾維血管擴張氣球導管許可證字號:衛署醫器輸字第020573號註銷狀態:註銷日期:註銷理由:有效日期:2025/02/01發證日期...

【亞培臨床生化載脂蛋白B檢驗試劑組(未滅菌)】許可證字號:衛署醫器輸壹字第005187號

器材品名:亞培臨床生化載脂蛋白B檢驗試劑組(未滅菌)許可證字號:衛署醫器輸壹字第005187號註銷狀態:註銷日期:註銷理由:有效日...

【閉塞氣球導管】許可證字號:衛署醫器輸字第009377號

器材品名:閉塞氣球導管許可證字號:衛署醫器輸字第009377號註銷狀態:已註銷註銷日期:2012/11/16註銷理由:許可證已逾有效期有...

【“美敦力”泰瑞斯可吸收式抗菌網袋】許可證字號:衛部醫器輸字第030303號

器材品名:“美敦力”泰瑞斯可吸收式抗菌網袋許可證字號:衛部醫器輸字第030303號註銷狀態:註銷日期:註銷理由:有效日期:2022/10/...

【內植用心臟整律器】許可證字號:衛署醫器輸字第000173號

器材品名:內植用心臟整律器許可證字號:衛署醫器輸字第000173號註銷狀態:已註銷註銷日期:2004/12/13註銷理由:未展延而逾期者...

【“美敦力”巧克力經皮腔內血管成形術球囊導管】許可證字號:衛部醫器輸字第033579號

器材品名:“美敦力”巧克力經皮腔內血管成形術球囊導管許可證字號:衛部醫器輸字第033579號註銷狀態:註銷日期:註銷理由:有效日...

【"美敦力" 自體輸血系統套統組】許可證字號:衛署醫器輸字第010375號

器材品名:"美敦力"自體輸血系統套統組許可證字號:衛署醫器輸字第010375號註銷狀態:已註銷註銷日期:2016/11/15註銷理由:未展...

【“美敦力”泰瑞思可吸收式抗菌網袋】許可證字號:衛部醫器輸字第033848號

器材品名:“美敦力”泰瑞思可吸收式抗菌網袋許可證字號:衛部醫器輸字第033848號註銷狀態:註銷日期:註銷理由:有效日期:2025/08/...

【"波士頓科技"可拆卸式氣球導管】許可證字號:衛署醫器輸字第012872號

器材品名:"波士頓科技"可拆卸式氣球導管許可證字號:衛署醫器輸字第012872號註銷狀態:已註銷註銷日期:2018/05/17註銷理由:許...

【“波士頓科技”安博倫皮下植入式心律去顫器】許可證字號:衛部醫器輸字第027871號

器材品名:“波士頓科技”安博倫皮下植入式心律去顫器許可證字號:衛部醫器輸字第027871號註銷狀態:註銷日期:註銷理由:有效日期:...

【“麥新”索菲雅導管】許可證字號:衛部醫器輸字第030752號

器材品名:“麥新”索菲雅導管許可證字號:衛部醫器輸字第030752號註銷狀態:註銷日期:註銷理由:有效日期:2023/03/05發證日期:201...