Editor's Note The Food and Drug Administration (FDA), on July 13, posted a nationwide recall by Hospira Inc (a Pfizer Company) of one lot (DX9067) of Propofol Injectable Emulsion, USP (containing Benzyl alcohol), 100 mL single patient use glass fliptop vial. The recall was initiated because of visible particulate observed…

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Editor's Note This Canadian study finds that hospitals impacted by COVID-19 can reduce their surgical backlogs by scheduling elective surgeries on the weekends. Using machine learning algorithms, the researchers demonstrated that even after resuming their usual level of surgical cases, the wait list would not decrease without a substantial increase…

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Editor's Note The Food and Drug Administration on July 20 identified the recall by Smiths Medical of certain Medfusion 3500 and 4000 Syringe Infusion Pumps as Class I, the most serious. The recall was initiated because of eight software malfunctions that affect different serial numbers and software versions. There have…

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Editor's Note The Food and Drug Administration (FDA) on July 6 identified the recall by Getinge USA Sales Inc of its Flow-c and Flow-e Anesthesia Systems as Class I, the most serious. The recall was initiated after reports of cracked or broken on/off switchs on the systems’ suction units. If…

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Editor's Note According to a June 20 article published by JDSupra from law firm Waller Lansden Dortch & Davis, recent government action out of the Justice Department involving ambulatory surgery centers (ASCs) and anesthesia provider arrangements points "to a need to carefully vet these partnerships,” Becker’s ASC Review June 21…

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Editor's Note The Food and Drug Administration (FDA) on June 28 identified the recall by GE Healthcare of its CARESCAPE R860 Ventilator as Class I, the most serious. The recall was initiated because the ventilator backup batteries, including replacement backup batteries, may run out before they are expected to do…

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Editor's Note The Food and Drug Administration (FDA) on June 23 identified the recall by Baxter Healthcare Corporation of its Volara system with in-line ventilator adaptor as Class I, the most serious. The Volara system is used to clear mucus out of airways, expand lungs, and treat or prevent pulmonary…

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Editor's Note The Food and Drug Administration (FDA) on June 21 identified the recall by Draeger, Inc, of one lot (LT2103) of its SafeStar 55 Breathing System Filters as Class I, the most serious. The Breathing System Filter is used as part of a ventilator when a patient is under…

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  Editor's Note In this study, researchers from the Mayo Clinic, Rochester, Minnesota, find that the use of eye protection by health care workers (HCWs) is important in preventing patient-to-HCW transmission of COVID-19. Of 345 HCWs who had a significant occupational exposure to patients with COVID-19, nurses accounted for 55.8%,…

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Editor's Note The American Society of Regional Anesthesia and Pain Medicine (ASRA Pain Medicine) developed and published on May 23 recommendations clinicians should take during the current shortage of the iodinated contrast medium (ICM) iohexol. Contrast medium, according to ASRA Pain Medicine, is used to confirm accurate needle placement and…

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