Editor's Note The Food and Drug Administration, on June 12, identified the recall of the rechargeable Walnut Wearable Smart Thermometer as Class I, the most serious. BearCare, Inc, is recalling the thermometers after receiving reports of skin burns and irritation resulting from use of the device. The company reports five…

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Editor's Note The Joint Commission and National Quality Forum (NQF) announced, on June 12, that they are now accepting applications for the 2023 John M. Eisenberg Patient Safety and Quality Awards, through August 7. The annual Awards, which recognize major achievements by individuals and organizations that use innovative approaches to…

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Editor's Note The Food and Drug Administration (FDA), on June 5, identified the recall by Abiomed of specific Impella 5.5 with SmartAssist heart pumps as Class I, the most serious. The recall was initiated because of fluid leaking from the purge sidearm of the pump. If the leak issue is…

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Editor's Note The Joint Commission, on May 31, announced that it has added several new and revised elements of performance (EPs) for critical access hospitals (CAHs) that address restraint and seclusion, the complaint process, and unified and integrated structures for CAHs that are part of a multihospital system, effective June…

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Editor's Note In a recent study led by researchers at Cleveland Clinic in Cleveland, OH, mobilization after elective surgery was found to be associated with fewer postoperative complications and shorter lengths of stay (LOS), and is an important component of Enhanced Recovery After Surgery (ERAS) protocols. This retrospective observational study…

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Editor's Note The Food and Drug Administration (FDA), on May 25, identified the recall by SD BioSensor, Inc, of certain Pilot COVID-19 At-Home Tests as Class I, the most serious. The recall was initiated because the liquid solution in the test kit may be contaminated with bacteria such as Enterococcus,…

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Editor's Note The Food and Drug Administration (FDA), on May 24, identified the recall by Draeger Medical of the Seattle PAP Plus as well as VentStar and other breathing circuit/anesthesia kits as Class I, the most serious. The recall was initiated after finding that glued connections may loosen before or…

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Editor's Note The Food and Drug Administration (FDA), on May 22, identified the recall by ICU Medical of replacement batteries for its Plum 360, Plum A+, and Plum A+3 infusions systems as Class I, the most serious. The recall was initiated because a manufacturing defect substantially diminished how long the…

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Editor's Note ECRI, on May 18, announced the winners of its annual 2023 Alerts Impact Award. The Award is given to members of ECRI’s Alerts Workflow system for excellence in recall management. The system’s software is used by supply chain, clinical engineering, IT, pharmacy, lab, clinical departments, and ancillary-care points…

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Editor's Note Because there is limited data to guide return to driving recommendations for patients after surgery, researchers at the Massachusetts General Hospital, Boston, performed this nested case-crossover study to find if the risk of a motor vehicle crash increases after surgery, compared to before. The analysis included 70,722 licensed…

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