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Avanos Medical has recalled Cortrak*2 EAS because of reports of deaths and injuries caused by tube misplacements.
The US Food and Drug Administration has identified the Cortrak*2 of Avanos Medical's enteral access system (EAS), for recall as a Class II recall.
Avanos Medical feeding tube Avanos Medical A Class 1 recall is the most serious among three classes.
Avanos Medical recalls Cortrak*2 EAS following reports of injuries and death due to incorrect placements of nasogastric or nasal tubes.
The device was designed to assist medical professionals who are trained to place medical tube feedings in patients and offer the most current information about tube placement.
But, the incorrect placement of the nasogastric or nasoenteric, tubes can result in severe injuries or even death.
The company has recalled 629 devices distributed throughout the US between January 2016 to January 2022.
According to the recall communication the company said that in the year 2015, there have been more than 60 injuries and 23 deaths resulting from the incorrect placement or the use of a nasogastric feeding tube while using the Cortrak* 2 EAS.
Avanos Medical will make the necessary changes to the labeling of the device following the recall. Avanos Medical feeding tube This includes updating Cortrak*2 EAS's instructions and expected uses.
feeding tube placement These updated guidelines require users to ensure that the tube is placed as per the guidelines of the institution's prior to use.
Avanos Medical has its headquarters in Alpharetta Georgia. Cortrak 2 eternal access system Avanos Medical sells its products in more than 90 different countries.
In December of last year Avanos Medical entered into an agreement worth $160 million to acquire OrthogenRx. Avanos Medical feeding tube Avanos Medical successfully closed the acquisition of OrthogenRx on 20 January.
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