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Pfizer places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Presentation: 1g/100 mL, Single Patient Use Glass Fliptop Vial Product: Configuration/Count Propofol Injectable Emulsion, 100 mL Single Patient Use Glass Fliptop Vial The NDC, Lot Number, Expiration Date, and Configuration details for Propofol Injectable Emulsion are indicated below. It is a sterile, nonpyrogenic emulsion containing 10 mg/mL of propofol suitable for intravenous administration supplied in a Single Patient Use Glass Fliptop Vial. Propofol Injectable Emulsion is a terminally sterilized (TS) product. Propofol is an intravenous general anesthetic and sedation drug for use in the induction and maintenance of anesthesia or sedation.
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Hypersensitivity reactions and transmission of infectious disease can also occur. Risk Statement: Patients receiving the impacted product have a remote probability of experiencing potential adverse events, such as blockage of blood vessels, including decreased blood flow to the brain, heart attack, pulmonary embolus, and tissue necrosis. To date, Pfizer has not received reports of any adverse events associated with this issue for this lot. See More was distributed nationwide to wholesalers/hospitals in the United States from Jthrough July 24, 2020. Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion (containing benzyl alcohol), 100mL Single Patient Use Glass Fliptop Vial lot EA7470, to the user level due to visible particulates observed in two vials during annual examination of retention samples.