FDA recalls Abbott’s HeartMate 3 ventricular assist device after 2 deaths
The Class I recall is the second one for Abbott’s HeartMate 3 device this year and follows 70 injuries and two patient deaths.
The Class I recall is the second one for Abbott’s HeartMate 3 device this year and follows 70 injuries and two patient deaths.
The companies will integrate Medis Medical’s non-invasive coronary physiology test, Medis QFR, with GE HealthCare’s cardiology Allia Platform.
The medical devices industry continues to be a hotbed of patent innovation. Activity is driven by increased need for homecare,...
Profound wins FDA clearance for AI support to Tulsa system
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Industry takes: the importance of keeping healthcare businesses cybersecure
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