In this article, LeAnne Hester, chief marketing officer of TRIMEDX, shares five ways clinical asset management technology empowers hospitals to improve patient safety, reduce risk, and optimize their equipment fleet.
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Despite Philips getting the green light from the U.S. FDA to start repairing and replacing ventilators impacted by the company’s class 1 recall, the FDA exposed a possible safety risk concerning a replacement component.
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The U.S. FDA is providing an update related to the June 14, 2021, recall of certain Philips Respironics ventilators, continuous positive airway pressure (CPAP), and bilevel positive airway pressure (BiPAP) machines.
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A software error has prompted a Class I recall of the Zimmer Biomet Rosa One Brain platform, a robotic system that helps neurosurgeons position tools and implants during brain surgery.
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EQ2 and Ordr are partnering up for a new HEMS software integration designed to help boost cybersecurity and aid in the safety recall process, according to company officials.
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