Editor's Note The Association for the Advancement of Medical Instrumentation (AAMI) on January 18 released a revised American National Standard that includes new information for manufacturers and users of personal protective equipment (PPE). The new edition of “ANSI/AAMI PB70:2022, Liquid barrier performance and classification of protective apparel and drapes intended…

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When making decisions about technology and equipment, there is a tendency to focus on immediate productivity increases—or perhaps, practical aspects such as carrying out an implementation or training staff. But here is another major issue: how to maintain OR equipment once the warranty runs out. This is more complex than…

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Over my 40-year career—after starting at the bedside in surgical intensive care, moving to emergency medicine, and then to perioperative services—I have been fortunate to progress into executive leadership positions in academic medical center health systems and community hospitals, consult with a top global advisory firm, and now work in…

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The use of electrosurgical instrumentation is common in minimally invasive surgery (MIS). However, while these instruments are common, processing them is complex and time-consuming. Insulated electrosurgical instrumentation can cause patient harm, including an electrical burn, if there is a breach in the insulation. These instruments are designed to have an…

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Editor's Note ECRI on January 11 announced that it is launching a new monthly video series featuring healthcare insights from its experts. Each episode will include topics of relevance to healthcare leaders, including physicians, nurses, pharmacists, patient safety and risk management professionals, supply chain leaders, and biomedical engineers. The first…

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Editor's Note The Food and Drug Administration (FDA) on January 10 announced that it had recently issued two warning letters to Olympus Medical Systems Corporation and one of its subsidiaries, Aizu Olympus Co, Ltd, after facility inspections. The letters addressed violations related to medical device reporting (MDR) requirements and quality…

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Editor's Note Allina Health and software company Qventus partnered earlier this year to implement an artificial intelligence-based tool to help automate OR scheduling, according to a January 10 PR Newswire release, reports January 11 Becker’s Hospital Review. The tool has capabilities to integrate into electronic health record systems and uses…

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Editor's Note The Food and Drug Administration (FDA) on December 16 identified the recall by Teleflex and Arrow International, LLC, of its Arrow MAC Two-Lumen Central Venous Access Kits and Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen Central Venous Catheter (CVC) Kits as Class I, the most serious. The recall…

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Editor's Note This study led by epidemiologist Cori L. Ofstead, MSPH, and associates, St Paul, Minnesota, found visible damage and residue or debris in 100% of 25 processed flexible endoscopes, using a new visual inspection program that included magnification and borescopes. Fully processed endoscopes were examined twice during a 2-month…

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Editor's Note The Food and Drug Administration (FDA), on December 20, identified the recall by Arrow International, LLC, subsidiary of Teleflex, Inc, of its Arrow AutoCAT 2 and AC3 intra-aortic balloon pumps (IABPs) as Class I, the most serious. IABPs are used in patients having cardiac and non-cardiac surgery, and…

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