The recall includes tube sizes 2.0, 2.5, 3.0 and 3.5 millimeters which may not provide sufficient airflow and can increase risk of hypoxia, laryngeal swelling, cardiopulmonary arrest and organ ...
The FDA reported March 25 that Smiths Medical Inc., is recalling a series of oral and nasal endotracheal tubes because the diameters of the tubes may present with “a smaller diameter than expected.” ...
The 2015 American Heart Association (AHA) Guidelines Update for Cardiopulmonary Resuscitation (CPR) and Emergency Cardiovascular Care (ECC) made several new changes for pediatric care associated ...
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The Anchorfast oral endotracheal tube fastener is currently reported as a medical device shortage under sections 62.21 to 62.26 of the Medical Devices Regulations. For a full list of shortages, refer ...
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