Medtronic recalls aneurysm-treating device linked to four deaths
The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
MedTech Dive3d
Medtronic recalls embolization devices tied to 17 injuries, 4 deaths
Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...
Med Device Online5d
Key QMS Considerations For Your Medical Device Startup
A quality management system (QMS) can often become bloated and unwieldy. This expert helps you understand key QMS basics and ...
Medical Device Network on MSN3d
FDA tags Medtronic embolisation device recall as Class I
Medtronic initiated the recall of certain Pipeline Vantage embolisation devices in January 2025 following reports of four ...
insurancebusinessmag6d
Australian product recalls climb amid regulatory changes – Sedgwick
advanced reforms to regulatory classifications for software-based medical devices. Additionally, the TGA introduced updates to the Uniform Recall Procedure for Therapeutic Goods, which places ...
MedTech Dive1d
Smiths Medical recalls port implants, warns on endotracheal tubes
The business, acquired by ICU Medical in 2022, has been dealing with a series of recalls and quality issues over the past ...
MassDevice1d
Smiths Medical has a serious recall involving vein access ports
The FDA has labeled Smiths Medical's recall of ProPort Implantable Plastic Port as Class I, the most serious kind.
Medical Design & Outsourcing4d
De-risking medical device startups with a systematic approach to innovation
XBeta founder Frederick Kruger offers advice for medical device startups based on his firm's development of the Spiro Wave ...
Becker's Hospital Review3d
Medtronic recalls embolization devices; 4 deaths reported
Medtronic has recalled certain Pipeline Vantage Embolization Devices with Shield Technology due to an increased risk of ...
The Cardiology Advisor1d
Boston Scientific Recalls Accolade Pacemaker Devices
Boston Scientific has issued a recall of Accolade pacemaker devices due to an increased risk for permanently entering Safety Mode.
FDA classifies recall of Medtronic embolization devices as 'most serious'
The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", ...
The New York Times1d
The Learning Network
This month marks the fifth anniversary of the pandemic. We asked students how their lives are different today because of it. By The Learning Network President Trump abruptly stopped providing ...