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Avanos Recalls Cortrak*2 Over Potential Enteral Tube Misplacement
This has led to 60 injuries and 23 deaths.

The FDA has classified this as an Class I recall, which is the most serious type of recall. These devices could lead to severe injuries or even death.

Sam Brusco, Associate Editor05.16.22

The FDA has identified Avanos Medical's recall of its Cortrak*2 access device for use in the system. 629 devices that were distributed between 2016 until 2022 were recalls in the U.S., beginning on March 21.

Avanos Medical feeding tube Cortrak*2 assists clinicians in placing medical feed tubes into patients that require nutrition via the tube.

https://divulgaaqui.online/author/avanos-medicalfabm505/ Cortrak 2 eternal access system The recall was triggered by death and injury reports from patients after nasocentric/nasogastric tube misplacement. Cortrak 2 eternal access system The device is used to assist in placing these tubes. If a nasogastric, or nasoenteric tube is not correctly inserted it can cause damage to the vocal cords, lungs, or trachea, resulting in severe injury or death.

Cortrak 2 eternal access system According to Avanos' safety communications, there were 60 injuries and 23 fatalities related to this incident. The adverse events mentioned included perforation, respiratory failure and pneumonia, in addition to the pleural effusion.

This recall is used to revise Cortrak*2's instructions regarding use, intended usage and also remind users to verify tube placement in accordance with institutional guidelines prior to using the tube in order to provide nutrients.

Clinicians were also advised to attach the field-correction notice about the issue to the operating guideline and return the acknowledgement form that was included with the notice to Avanos. Avanos plans to provide users with current labeling, which will include confirmation of tube placement in accordance with the institution's policies prior to use.


Website: https://divulgaaqui.online/author/avanos-medicalfabm505/