FDA classifies recall of Medtronic’s HeartWare HVAD batteries as Class I
The firm recalled the HeartWare Ventricular Assist Device (HVAD) system batteries due to risks of electrical faults that…
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26 Aug 22
The firm recalled the HeartWare Ventricular Assist Device (HVAD) system batteries due to risks of electrical faults that…
29 Jun 22
The CARESCAPE R860 ventilator's backup batteries and replacement backup batteries were recalled as they were draining fast and…
17 May 22
The Cortrak* 2 EAS device has been designed to help health care professionals to place the medical feeding…
The US engineering firm's cyber security programme will initially provide specialised training for medical device manufacturers via online…
The FDA has issued a do-not-use list of 'dangerous' hand sanitiser products thought to be contaminated with toxic…
21 Apr 20
The company has determined that one (1) isolated TRUE METRIX AIR Blood Glucose Meter was packaged into a…
31 Mar 20
The Global Medical Device Nomenclature Agency's international naming system will help the NHS use barcode data to improve…
The MHRA says it has received reports of the Emerade auto-injector pen failing to activate, meaning children may…
Medical device failures can have adverse consequences for healthcare professionals, as well as patients, in certain cases
17 Feb 20
These recalled products were manufactured from October 2014 through June 2019