Supply Chain/Technology
FDA: Class I recall of Amsorb Plus used to absorb carbon dioxide in anesthesia machines
Editor's Note The Food and Drug Administration (FDA), on September 23, identified the recall by Armstrong Medical of certain lots of its Amsorb Plus Prefilled G-Can 1.0L canisters as Class I, the most serious. Amsorb Plus is a chemical substance used in anesthesia machines to absorb carbon dioxide the patient…
ECRI partners with FDA on safety of materials in medical devices
Editor's Note ECRI, on September 30, announced a new partnership with the Food and Drug Administration (FDA) to improve the safety of medical devices through the use of safer materials. ECRI is developing safety reports for materials commonly used in implantable medical devices and assessing their possible effects on patients…
How might telehealth alter approaches to surgical patient care?
Telehealth services grew exponentially in the early days of the COVID-19 pandemic. Overall telehealth utilization for office visits and outpatient care was 78 times higher in April 2020 than in February 2020, according to a McKinsey & Company July 2021 report. Since then, telehealth utilization has stabilized at levels that…
FDA: Class I recall of Normoflo irrigation fluid warmers, warming sets
Editor's Note The Food and Drug Administration (FDA) on September 15 identified the recall of Smiths Medical Normoflo irrigation fluid warmers and warming sets as Class I, the most serious. The recall was initiated because of the potential for aluminum ions leaching into warmed fluids, potentially exposing patients to high…
Zimmer Biomet platform links with Apple Watch for postop patient care
Editor's Note Zimmer Biomet on August 31 presented data at the American Academy of Orthopaedic Surgeons 2021 annual meeting that highlighted the clinical value of its MyMobility platform with Apple Watch, the August 31 Mass Device reports. MyMobility is a remote care management platform that helps guide and support patients…
FDA: Cardinal Health recalls Monoject Saline Flush Prefilled Syringes
Editors Note The Food and Drug Administration (FDA) on August 23 identified the recall by Cardinal Health of its Monoject Saline Flush Prefilled Syringes as Class I, the most serious. Cardinal Health is recalling three models of the syringes because the syringe plunger may pull air into the syringe after…
AORN to launch ‘Center of Excellence in Surgical Safety: Prevention of RSI’
Editor's Note AORN announced on August 15 that it will launch a new “Center of Excellence in Surgical Safety: Prevention of RSI.” Facilities will be recognized as Centers of Excellence for implementing a surgical team-based program to prevent retained surgical items (RSI). The complimentary program, sponsored by the AORN Foundation…
Use of targeted behavioral science messages to increase HCW COVID-19 vaccinations
Editor's Note In this study by researchers at Geisinger Health System, Danville, Pennsylvania, an individually addressed email nudge designed with behaviorally informed features caused more than twice as many healthcare workers (HCWs) to register for a COVID-19 vaccination, compared with HCWs in a control group. The health system initially sent…
Cigna, Oscar Health to offer virtual-first primary care plan
Editor's Note Cigna and New York City-based Oscar Health will offer a virtual-first primary care plan next year in Georgia and Tennessee for small businesses, the July 22 Becker’s Hospital Review reports. The model, which will be available on some of the insurers’ joint plans, offers unlimited primary care provider…
ECRI partners with Nuvolo on standardization of device data
Editor's Note ECRI on July 20 announced a collaborative partnership with Nuvolo, an independent software vendor involved in cloud-based connected workplace solutions, based in Paramus, New Jersey. The partnership integrates ECRI’s standardization of medical device data with Nuvolo’s Connected Workplace for Healthcare. This automated process enables standardization of device data…
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