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Avanos Recalls Cortrak*2 Over Potential Enteral Tube Misplacement
This issue is responsible for at the very least 60 injuries and 23 fatalities.

The FDA has declared this to be an Class I recall, the most serious type of recall. Cortrak 2 eternal access system The use of these devices could cause serious injuries or death.

Avanos Mediacal Cortrak 2 Sam Brusco is Associate Editor05.16.22

The FDA has identified Avanos Medical’s recall its Cortrak*2 useal access system. The recall of 629 devices that were distributed from 2016 to 2022 began on March 21.

Cortrak*2 helps clinicians place medical feeding tubes inside the stomach or in the small bowel of patients who require nutrition via tube.

Due to the possibility of injuries or deaths, the system was recalled. feeding tube placement Nasogastric, also known as nasoenteric, tube that is not correctly inserted can cause damage to the vocal chords and trachea. This can lead to severe injury or death.

According to Avanos the safety communication the number of injuries was 60 and 23 deaths related to this incident. Some of the adverse events reported were pneumothorax, respiratory failure perforation, pneumonia, and the pleural effusion.

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 nutrition.

feeding tube placement Avanos Medical feeding tube Clinicians were also encouraged to attach the corrected note in the field on the issue to Avanos operating manual and to return the acknowledgement forms with Avanos' notice. The company hopes to soon provide users with updated labeling. This includes confirmation that tube placement was carried out in accordance with institutional policy.


My Website: https://www.mpo-mag.com/contents/view_breaking-news/2022-05-16/avanos-recalls-cortrak2-over-potential-enteral-tube-misplacement