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Avanos Medical, FDA and the FDA have issued an Class 1 Recall of approximately 629 units CORTRAK*2 Ental Access System. Cortrak 2 eternal access system This feeding tube positioning device has been linked to numerous deaths and injuries.
The devices that were recalled were released between April 1 2016, 2016 until January 1, 2022. Avanos Medical They're used to aid healthcare professionals to insert feeding tubes into the stomach or the intestines of patients.
Avanos Mediacal Cortrak 2 Avanos Mediacal Cortrak 2 The incorrect placement of the nasogastric tube and Nasoenteric tube was the source of 53 deaths and 60 injuries since the year 2015.
Avanos Medical feeding tube This recall is used to update the information on the device, in order to remind users to ensure that the tube has been set before they can provide the food.
https://www.medtechdive.com/news/avanos-medical-recall-class-i/623892/ According to FDA, adverse events included respiratory failure and pneumothorax (collapsed lung tissue), perforation [a hole in the bowel or wall of the lungas well as pneumonia (a lung infection), and Pleural effusion (excess fluid in the lung space and the chest cavity).
Avanos Medical feeding tube 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]. Avanos Medical
Here's my website: https://www.afslaw.com/perspectives/investigations-blog/medical-device-company-pays-38-million-resolve-criminal-charges
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