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Avanos Recalls Cortrak*2 Over Potential Enteral Tube Misplacement
There are 60 reported injuries and 23 deaths related to this problem.

Avanos Medical feeding tube The recall is classified by FDA as a class I recall. Avanos Medical feeding tube This is the most serious form of recall. These devices could cause grave injuries, and possibly death.

Cortrak 2 eternal access system Sam Brusco Associate Editor05.16.22

The FDA has identified Avanos Medical’s recall of its Cortrak*2 intramuscular accessibility system. 629 devices, distributed from 2016 and 2022 were recalled by the U.S. starting on March 21.

Avanos Medical Cortrak*2 assists clinicians in placing medical feeding tubes into the stomach or small bowels of patients that need to be fed via the tube.

Due to the possibility of injuries or deaths, the system was recalled. Incorrectly inserting an Nasogastric tube or Nasoenteric one can cause serious injury or even death.

Avanos Medical feeding tube Cortrak 2 eternal access system According to Avanos reports, there were more than 60 injuries and 23 deaths in connection with this issue. The adverse events that were reported include respiratory failure, pneumothorax, perforation, pneumonia and pleural effusion.

Avanos Mediacal Cortrak 2 Cortrak 2 eternal access system Cortrak*2 will utilize the recall to revise its guidelines for use and intended use. It will advise users to verify tube placement with the help of institutional protocols prior to providing food.

Clinicians were requested to attach the notice of correction regarding the issue to the operating book and return the acknowledgement form with the note to Avanos. The company plans to offer users the most current labeling, along with confirmation of tube placement in accordance with the institutional guidelines.


Website: https://www.massdevice.com/avanos-medical-recall-of-cortrak-2-enteral-access-system-is-class-i/