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There were 60 injuries as well as 23 deaths as a result of this problem.
https://www.medicaldevice-network.com/news/fda-avanos-medical-cortrak2-eas-recall/ The FDA has identified this as an Class I recall, which is the most serious kind of recall. The devices could cause grave injuries, or even death.
Sam Brusco, Associate Editor05.16.22
The FDA has discovered Avanos Medical's recall of its Cortrak*2 intramuscular access system. Starting on March 21 the 21st of March, 2016, 629 devices were recalls in the U.S.
Cortrak*2 assists clinicians in placing medical feeding tubes inside the stomach or in the small bowels of patients needing to receive nutrition through the tube.
The device was temporarily recalled because of injuries and death reports resulting from nasocentric and nasogastric tube misplacement when it is employed to help place these tubes. https://www.nsmedicaldevices.com/news/avanos-medical-cortrak-2-eas-class-i-recall/ If a nasogastric or nasoenteric tube is not correctly inserted it can cause damage to the vocal cords, lungs or the trachea, leading to serious injury or death.
Avanos Medical feeding tube According to Avanos Safety communications the number of injuries was 60 and 23 deaths related to this issue. The adverse events that were reported include pneumothorax, respiratory failure, perforation, pneumonia, as well as the development of pleural effusion.
Cortrak 2 eternal access system This recall is used to revise Cortrak*2's instructions for use, intended uses and also advise users to verify tube placement in accordance with institutional guidelines prior to using the tube in order to supply nutrition.
Cortrak 2 eternal access system Clinicians were directed to attach the pertinent field correction notice to their operating manual. feeding tube placement They should also return the acknowledgement slip included with the Avanos note. The company plans to offer users the most current labeling and also a confirmation of tube placement according to the policies of the institution.
Website: https://www.medscape.com/viewarticle/891200
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