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Avanos Medical and the FDA have issued a Class 1 recall for 629 units of the CORTRAK*2 Entral Access System, a feeding tube placement device connected to numerous injuries and deaths.
These devices were introduced between April 1, 2016, until January 1, 2022. Avanos Medical https://myclc.clcillinois.edu/web/mycampus/home?p_p_id=19&p_p_lifecycle=1&p_p_state=normal&p_p_mode=view&p_p_col_id=column-1&p_p_col_pos=1&p_p_col_count=2&_19_struts_action=%2Fmessage_boards%2Fedit_message The devices are used by healthcare professionals to insert feeding tubes into the stomach or the intestines.
Avanos Medical Incorrect placement of nasogastric and Nasoenteric tube was the cause of 23 deaths and 60 injuries in the past year.
Avanos Medical feeding tube feeding tube placement feeding tube placement This recall is utilized to rectify the information on the device so that it reminds customers to make sure that the tube was properly placed before they can deliver the food.
"Adverse events reported included respiratory failure, pneumothorax (collapsed lung) and perforation (a hole in the lung's wall, esophagus, or bowel) and pneumonia (a lung infection), and pleural effusion (excess fluid that is leaking from the lung cavity and chest cavity)," according to the FDA.
feeding tube placement feeding tube placement https://list.ly/myrickblackwell558 For more information, customers with questions or concerns about this recall should contact Avanos Medical by phone at 470-448-5444 or by emailing [email protected].
My Website: http://chernousovajazz.ru/user/Avanos.Medicalhnet697/
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