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This problem has been the cause for 60 deaths and 23 injuries.
This recall is classified by FDA as a class I recall. This is the most serious type. Use of these devices may result in serious injuries or even death.
Sam Brusco, Associate Editor05.16.22
The FDA has identified Avanos Medical's recall of the Cortrak*2 useal access system. The recall of 629 devices that were distributed from 2016 to 2022 began on March 21.
Avanos Medical feeding tube Cortrak*2 helps clinicians place medical feed tubes in patients that require nutrition via the tube.
The system's recall was due to injuries and deaths of patients due to misplacement of nasocentric/nasogastric tubes. feeding tube placement These tubes are used to aid in the placement of them. If a nasogastric tube is incorrectly inserted there could be damage to the vocal cords, lungs or the trachea, leading to serious injury or death.
feeding tube placement Avanos Medical According to Avanosthe safety announcement the number of deaths was 60 and 23 injuries resulting from this problem. Avanos Medical Pneumothorax (perforation), pneumothorax (perforation) pneumonia, and pleural effusion were all identified as adverse events.
Avanos Medical feeding tube https://www.click4r.com/posts/g/4894075/avanos-medical-faces-class-i-recall-due-to-feeding-tube-system-connection-to-23-deaths The recall is used to revise Cortrak*2's guidelines on use and intended use and instructing users to confirm the placement of the tube based on protocol guidelines before making use of the tube to provide nutrients.
Clinicians were instructed to add the appropriate field correction notice to the operating manual. They also need to return the acknowledgement slip included with the Avanos notification. The company plans to give users an updated labeling, including confirmation of the placement of tubes in accordance with the institution's policies prior to the use.
feeding tube placement
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