Editor's Note The Food and Drug Administration (FDA) on August 22 posted the Hospira Inc (a Pfizer company) recall of one lot of Propofol Injectable Emulsion (containing Benzyl alcohol), 100 mL single patient use glass fliptop vials, lot EA7470. The recall was initiated because of visible particulates observed in two…
Editor's Note The Food and Drug Administration (FDA) on August 19 identified the recall by Medtronic of its Cobalt XT, Cobalt, and Crome Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) as Class I, the most serious. The devices are being recalled because of reports of short circuit-protection…
What if unprofessional behavior in the OR could be managed through something as simple as an informal chat over a cup of coffee? This peer-to-peer approach advocated by Vanderbilt University School of Medicine led to the development of two well-established, scientifically validated programs designed to offset unprofessional behavior: the Patient…
Editor's Note This study led by researchers at Cedars-Sinai Medical Center, Los Angeles, finds that more than half of adults with recent Omicron infection analyzed were unaware of their infectious status. Of 210 adult employees or patients at Cedars-Sinai Medical Center with serological evidence of recent Omicron variant infection: 92…
Editor's Note This study led by researchers at State University of New York Downstate Health Sciences University, Brooklyn, finds that patients having major surgical procedures within 8 weeks of a COVID-19 infection have a substantially higher postoperative 90-day mortality, regardless of symptoms. Analyzing data on 938 COVID-19 positive patient cases…
Editor's Note This retrospective cohort study led by researchers at Ascension Health, St Louis, finds that COVID-19 infection is a risk factor for adverse peripartum maternal outcomes. Researchers evaluated the association of COVID-19 with severe maternal morbidities in patients delivering during four pandemic periods characterized by predominant variants—March-December 2020 (wild…
Editor's Note The Food and Drug Administration (FDA) on August 11 classified the recall by Becton Dickinson (BD) of its Intraosseous Infusion System, which includes Intraosseous Needle Set Kits, Intraosseous Manual Driver Kits, and Intraosseous Powered Drivers, as Class I, the most serious. The recall was initiated for three separate…
Editor's Note This meta-analysis led by researchers at the National University of Singapore finds that recovery of the ability to taste and smell after COVID-19 infection may take up to 6 months, and women are more likely to experience loss of these senses and have a longer time to recovery.…
Editor's Note The Food and Drug Administration (FDA) on August 9 identified the recall by Haimen Shengbang Laboratory Equipment Co Ltd of its Viral Transport Media Containers as Class I, the most serious. The recall was initiated because the products were distributed in the US without authorization, clearance, or approval…
Editor's Note This study led by researchers at the University of California, San Diego, finds that healthcare facilities in counties with higher Black composition and rural areas with large Hispanic populations were less likely to serve as COVID-19 vaccine administration locations during the initial rollout in May 2021. At that…