Medtronic initiates recall for silicone-based EMG endotracheal tubes due to the risk of airway obstruction and ventilation failure.
Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and inadvertently shipped to certain stores on or around May 1, 2022 through June 10, 2022 due to product being stored outside of labeled
Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and shipped to a limited number of stores in AZ, CA, GA, ID, IN, MT, NM, NV, OR, TX, and UT on or around May 1, 2022 through June 21, 202
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Le vériciguat est indiqué dans le traitement de l'insuffisance cardiaque chronique symptomatique pour diminuer les risques de décès cardiovasculaire et d'hospitalisation liés à l'insuffisance cardiaque, chez l'adulte à fraction d'éjection de moins de 45 % dont l'état est stabilisé après une décompensation récente de l'insuffisance cardiaque. Le vériciguat devrait être utilisé en combinaison avec d'autres traitements de l'insuffisance cardiaque.
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