Medtronic’s HeartWare Receives Another Class I Recall After More Patient Deaths
This recall, linked to two patient deaths, is the third in 12 months for Medtronic’s HeartWare HVAD ventricular assist device, reports MedTech Dive.
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Hillrom Patient Lift Tied to 2 Deaths, Designated as Class I Recall
Hillrom’s recalled Liko Multirall 200 overhead patient lift has been linked to two deaths and there are more than 20 reports of serious injuries, reports MedTech Dive.
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ECRI, oneSOURCE Collaborating to Improve Medical Device Alerts Management
The new integration enables biomedical engineers to respond more quickly to device safety issues in an era of COVID-19.
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Transitioning from Field Service to the Hospital
In this Soapbox article, George Pazak, a BMET III at Methodist Hospital in Indiana, details how he transitioned from field service to the hospital and advises others looking to do the same.
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FDA 2020 Recall Roundup: A Rough Year for Infusion Pumps
Infusion pumps or their components account for nine entries in the FDA’s list of 2020 medical device recalls.
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