Supply Chain/Technology

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November 2025
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Johns Hopkins robot performs first laparoscopic intestinal anastomosis without human help

Editor's Note The Smart Tissue Autonomous Robot (STAR), designed by a team of researchers at Johns Hopkins University, has performed laparoscopic intestinal anastomoses in four experiments on pig tissue without human help. The robot outperformed surgeons using manual-laparoscopic and robot-assisted surgical techniques in the consistency of suture spacing and bite…

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By: Judy Mathias
January 31, 2022
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Creating work schedules with AI reduces physician burnout

Editor's Note Artificial intelligence (AI)-based scheduling significantly improved physician engagement and reduced burnout, in this study presented by Ochsner Health researchers, January 28, at the American Society of Anesthesiologists’ ADVANCE 2022, the Anesthesiology Business Event, in Dallas. The AI-based scheduling software, which created fair and flexible schedules that supported work-life…

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By: Judy Mathias
January 31, 2022
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The Joint Commission revises Environment of Care Chapter

The Joint Commission revises Environment of Care Chapter The Joint Commission on January 26 announced that it has approved several revisions to Elements of Performance (EP) in the Environment of Care (EC) chapter, which will vary across accreditation programs. Among the revisions: Standard EC.02.04.01, EP 11, which addresses reporting incidents…

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By: Judy Mathias
January 27, 2022
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Incidental COVID-19 hospital cases are hard to track

Editor's Note Incidental COVID-19—when patients are admitted to the hospital for something other than COVID-19 but test positive for the virus during their stay—is a reality for most, if not all, hospitals. However, a Becker’s study finds that the frequency of incidental COVID-19 cases is particularly challenging for hospital staff…

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By: Tarsilla Moura
January 25, 2022
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FDA: Class I recall of Getinge Vaporizer Sevoflurane Maquet Filling for Flow Family Anesthesia Systems

Editor's Note The Food and Drug Administration (FDA) on January 19 identified the recall by Getinge of its Vaporizer Sevoflurane Maquet Filling for Flow Family Anesthesia Systems as Class I, the most serious. The recall was initiated because of the potential chemical breakdown of Sevoflurane that may result in inhalation…

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By: Judy Mathias
January 20, 2022
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Integrated data, insights lead to cost, time savings for OR staff

In 2020, supply costs were once again reported as one of the greatest line-item expenses in a hospital, exceeding labor expenses. US hospitals have most recently reported a combined $36 billion in medical and surgical supply costs. These expenses account for more than half of a hospital’s total supply costs.…

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By: Shawn McBride
January 20, 2022
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ECRI names Top 10 Health Technology Hazards for 2022

Editor's Note ECRI has named cybersecurity attacks as the number one health technology hazard for 2022. In its report, ECRI notes that all healthcare organizations are subject to cybersecurity attacks, and that the question is not whether they will be attacked but when. A cybersecurity attack could threaten medical devices…

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By: Judy Mathias
January 19, 2022
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FDA: Class I recall of Medtronic Synergy Cranial, StealthStation S7 cranial software

Editor's Note The Food and Drug Administration (FDA) on January 6 identified the recall by Medtronic of its Stealth Station System with Synergy Cranial and StealthStation S7 Cranial Software as Class I, the most serious. The System aids in precisely locating anatomical structures in neurosurgical procedures. The recall was initiated…

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By: Judy Mathias
January 18, 2022
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FDA: Class I recall of Cardiovascular Systems’ WIRION Embolic Protection Device

Editor's Note The Food and Drug Administration (FDA), on January 10, identified the recall of Cardiovascular Systems’ WIRION Embolic Protection Device as Class I, the most serious. The device, which is used to hold or remove debris or blood clots from the lower limbs, was recalled because of complaints of…

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By: Judy Mathias
January 11, 2022
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FDA: Class I recall of Puritan Bennett 980 Series Ventilator

Editor's Note The Food and Drug Administration (FDA), on January 3, identified the recall by Covidien of its Puritan Bennett 980 Series Ventilator as Class I, the most serious. The recall was initiated because of a capacitor manufacturing assembly error that may cause the ventilator to become inoperable or stop…

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By: Judy Mathias
January 5, 2022
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