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Avanos Medical Cortrak*2 enteral access system was designed to allow health professionals to place medical feeding tubes into the small intestine or stomach of patients that require nutrition. Cortrak 2 eternal access system However, since 2015, there has been 23 deaths attributed to the feeding tube.
There have been numerous reports of injuries to patients and deaths resulting from misalignment or misplacement of nasogastric, also known as nasoenteric, tubes. They are employed to assist in the placement of their tubes.
Cortrak 2 eternal access system The recall was used to create changes to the labels of the device and instructions for use and intended purpose. It is recommended that users verify that the tube has been placed in accordance with the specifications of their institution before using it to deliver nutrition.
The incorrect placement of a Nasogastric or Nasoenteric tube may cause harm to the vocal cords, lungs, or trachea. This could result in serious injury and even the death.
Avanos Medical Avanos Medical's recall communications declared that there had been sixty accidents, 23 deaths and 58 patients who were hurt by the misplacement of nasogastric tubes. The CORTRAK*2 access device has been used since the year 2015. https://www.fdanews.com/articles/203704-avanos-medical-to-pay-22-million-settlement-over-misbranded-surgical-gowns There were a variety of adverse events, such as respiratory failure, pneumothorax (collapsed lung tissues) as well as perforation (a gap or opening in the esophagus's wall or the bowel) as well as pneumonia and pleural effusion (excess fluid in the air space between your lungs and the chest cavity).
Avanos Medical, on March 21, 2022, sent a field correct notification to its customers who had used the products between January 2021-January 2022. Avanos Medical feeding tube Cortrak 2 eternal access system The notice included these instructions:
Confirm placement of nasogastric and nasoenteric tubes according to institutional policies.
Cortrak 2 eternal access system Attach the correction notice from the field that explains the issue to the operator's manual.
Avanos will need to acknowledge the receipt of the email notification.
Here's my website: https://biotech-insider.com/avanos-medical-faces-class-i-recall-for-feeding-tube-system-linked-to-23-deaths-since-2015/
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