In the Enforcement Report for the week of January 23 the FDA lists the voluntary Class II Recall by Philips Medical Systems (Cleveland) Inc of the computed tomography x-ray system Brilliance workspace portal.
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The Government Accountability Office (GAO) is launching an investigation into the U.S. FDA’s potentially ineffective policies for recalling medical devices, prompted by concerns raised by Senators Durbin and Blumenthal regarding the slow response to recalls of Philips Respironics CPAPs, BiPAPs, and mechanical ventilators.
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Sustainability is about reducing wastefulness and anyone in HTM can contribute to that goal with the right mindset.
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The Canadian government’s response to ventilator needs of patients early during the pandemic resulted in an excessive equipment surplus.
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Intuitive measures to curb the initial unpreparedness for the pandemic resulted in the inflow of mechanical ventilators at the expedited rate.
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