Medical Recalls Medtronic

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Medtronic Recalls MiniMed Insulin Pumps for Incorrect …

https://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-minimed-insulin-pumps-incorrect-insulin-dosing

Medtronic is recalling the specified insulin pumps to replace any pump that has a clear retainer ring with one that has the updated black retainer ring at no charge. A replacement insulin pump will be provided even if the clear retainer ring is not damaged and regardless of the warranty status of the pump. Medtronic … See more

2022 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls

Medtronic Recalls Cobalt XT, Cobalt and Crome ICDs and CRT-Ds for Risk that Devices May Issue a Short Circuit Alert and Deliver Reduced Energy Shock During High …

2021 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2021-medical-device-recalls

Dec 16, 2021

Medtronic Recalls ICDs, CRT-Ds for Risk of Shortened …

https://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-evera-viva-brava-claria-amplia-compia-and-visia-implantable-cardioverter

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

Medtronic Recalls Mahurkar High Flow Catheters for …

https://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-mahurkar-acute-dual-lumen-high-flow-hemodialysis-catheters-potential-catheter-hub/

Medtronic Recalls Mahurkar Acute Dual Lumen High Flow Hemodialysis Catheters for Potential Catheter Hub Defect | FDA Medtronic Recalls Mahurkar Acute …

Recalls | Medtronic

https://global.medtronic.com/xg-en/e/response/recalls.html

The FDA explains that “[a] medical device recall does not always mean that you stop using the product or return it to the company,” and a recall can include “inspecting the device …

Medtronic sees 23 serious medical device …

https://www.msn.com/en-us/health/medical/medtronic-sees-23-serious-medical-device-recalls-in-two-years/ar-AA15t1SN

Medtronic, with fiscal 2022 sales of $31.7 billion, is the largest medical device manufacturer in the industry, which puts it at higher recall risk because it …

Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls

The FDA posts summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that …

Dual Chamber Pacemakers: Urgent Medical Device …

https://www.medtronic.com/us-en/healthcare-professionals/products/product-performance/dual-chamber-pacemaker-recall.html

Medtronic records indicate that your facility may have product inventory potentially affected by this issue. As a result, Medtronic requests that you immediately take the following …

GE HealthCare Recalls Nuclear Medicine 600/800 …

https://www.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients

See Medical Device Recall Database entry for more information. Distribution Dates: April 1, 2018 to December 16, 2022; Devices Recalled in the U.S.: 688; Date …

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