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Avanos Medical and the FDA have issued a Class 1 recall for about 629 units of the CORTRAK*2 Enteral Access System, a feeding tube placement device responsible for dozens of injuries and deaths.
The devices for recall were distributed between April 1, 2016 to January 1, 2022. https://www.fcc.gov/fcc-bin/bye?https://medicaldevices.icij.org/devices/hkg-cortrak-2-enteral-access-system-eas These devices can be utilized by healthcare professionals to place feeding tubes inside the stomach or in the intestines.
https://peatix.com/user/14353944 Incorrect placement of the nasogastric or nasoenteric tube has been the cause of 23 deaths and 60 injuries since 2015.
Avanos Mediacal Cortrak 2 The recall is used to change the label on the device to remind users to check that the tube has been correctly placed before delivering nutrition.
According to FDA adverse events, they include respiratory failure, pneumothorax (collapsed lungs) Perforation (a hole in the wall or bowel of the lungas well as pneumonia (a lung infection) and the pleural effusion (excess fluid in the space between your lungs and the chest cavity).
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]. https://500px.com/p/wittavvklemmensen https://www.misterpoll.com/users/avanos mediacal cortrak 2zgvg7935
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