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This issue is responsible for at least 60 injuries and 23 fatalities.
Avanos Mediacal Cortrak 2 https://500px.com/p/godwinrzcmccarty This is an item classified as a Class I recall by FDA, which is the most serious type. Use of these devices may cause serious injury or death.
Sam Brusco is Associate Editor05.16.22
The FDA has discovered Avanos Medical's recall of Cortrak*2 entry access system. 629 of the devices produced between 2016 to 2022 were recalled the first recall taking place on the 21st of March.
Cortrak*2 helps clinicians place medical feeding tubes into the stomachs or small bowels of patients who require to be fed via the tube.
In the wake of deaths and injuries caused by the system, it was removed. A wrongly placed nasogastric or nasal tube can cause serious injury or death.
According to Avanos’ safety communication, there were 60 deaths and 23 injuries that were related to the issue. https://www.pinterest.com/avanos medicallwpd838/ Adverse events reported included pneumothorax, respiratory failure, perforation, pneumonia, as well as the pleural effusion.
Cortrak*2 has utilized the recall to make changes to its instructions for use. https://escatter11.fullerton.edu/nfs/show_user.php?userid=2740268 The new instructions contain instructions for users to verify that tubes are placed in accordance with the guidelines of the institution before applying them to provide nutrition.
feeding tube placement Clinicians were advised to attach the corrective field notice regarding the issue to their operating manual and to return the acknowledgement form which was included in the notice to Avanos. The company aims to soon provide users with new labeling and confirmation of the placement of tubes in accordance with the institution's policies prior to use.
My Website: https://escatter11.fullerton.edu/nfs/show_user.php?userid=2740268
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