The company began the recall after receiving four field complaints about tip separation before and during use.

The medical cannula market is experiencing consistent growth, driven by the global demand for advanced medical devices and ...

This two day interactive seminar will focus on: Complaint Management Medical Device Reporting (MDR) EU Vigilance Reporting Product Recalls This course will provide practical guidance and real life ...

Medtronic Embolization Devices: The recall impacts the Pipeline Vantage devices compatible only with 0.027" inner diameter microcatheters, Medtronic said. The company added that it has taken the ...

The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as Class I following reports of four patient deaths. A Class I recall is the ...

3 medical device recalls and corrections Medical device recalls are essential to patient safety, addressing critical issues in devices that may pose health risks. Advertisement By: Alexandra Murphy ...

The need to build an effective recall management team in health care is becoming increasingly clear. Consider the recent news that medical device recalls by the Food and Drug Administration reached a ...

Meeting Coverage > STS Limbo of Cardiac Device Recalls Has Physicians Ready for Change — How innovation may play out under Trump, and medicolegal implications of using recalled devices by Nicole ...

A new process that consolidates machine learning algorithms with unique human-based expertise promises to improve the regulatory and approval process for new medical devices by reducing the recall ...

Spotlighting the issue is a new study in the Annals of Internal Medicine looking at recalls of heart devices -- like pacemakers, stents, and defibrillators -- from 2013 to 2022. It found 157 heart ...