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Avanos Medical has recalled the Cortrak*2 Ental Access System because of accidents and deaths that result from misplacement of nasoenteric and nasogastric tube. Cortrak 2 eternal access system The recall covers 629 devices which were distributed throughout the United States.
Avanos has marketed the Cortrak*2 Entraal Access System that assists with the installation of a medical-feeding tube. Patients can suffer from harm to their vocal cords or trachea, if the tube has been installed improperly. Avanos Medical recalls that there were 60 accidents, 23 deaths, and 23 illnesses that were caused by the improper placement or accidental inserting of nasogastric feeding tube while using the CORTRAK*2 Entral Access System. Pneumothorax (collapsed lung) or pneumothorax, perforation (a gap or hole within the lung's wall) as well as pneumonia. feeding tube placement https://musescore.com/user/52683926 Pleural effusion (excess liquid between the chest cavity and the lungs) are some of the incidents.
https://www.transtats.bts.gov/exit.asp?url=https://24x7mag.com/standards/fda-updates/avanos-medicals-enteral-access-system-gets-fda-class-i-recall/ Cortrak 2 eternal access system Avanos Medical has presented a plan to update users' labels, to ensure the proper place of the nasogastric (and nasal) tubes prior to using them.
The Avanos warning was the second FDA warning in 2022 regarding tube feeding for enteral use. In February the FDA issued a warning to healthcare professionals as well as parents about the possibility of strangulation when children use feeding tubes. Two deaths resulting from strangulation of children took place in 2021 because of a tube that was tied around the neck of a child.
FDA Recalls Avanos Medical Device
Potential Risks in Enteral Feeding Delivery sets
Cortrak* 2 Enteral Access System Product Details
CONTACT PARKER WAICHMAN LLC FOR A FREE CASE VIEW
Have you or someone you love suffer injury from a recalled product? Parker Waichman LLP helps those who've suffered injuries making use of vehicles that are defective receive financial compensation. Our product litigation lawyers will take charge of your case. To schedule a consultation for free, please contact our law office today by live chat or calling 1-800-YOURLAWYER (1-808-968 7529).
Homepage: https://www.transtats.bts.gov/exit.asp?url=https://24x7mag.com/standards/fda-updates/avanos-medicals-enteral-access-system-gets-fda-class-i-recall/
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