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This issue has been responsible for the deaths of 60 and 23 injuries.
The recall has been classed by FDA as a class I recall. This is the most serious form of recall. These devices could cause serious injuries or even death.
Sam Brusco, Associate Editor05.16.22
The FDA has discovered Avanos Medical's recall of its Cortrak*2 intramuscular accessibility system. 629 devices manufactured between 2016 to 2022 were recalled the first recall taking place on the 21st of March.
Cortrak*2 lets clinicians insert medical feeding tubes into the stomach or small bowel of patients who require nutritional assistance.
Avanos Medical feeding tube Due to injuries and deaths, the system was recalled. Nasogastric, also known as nasal, tube that is not correctly inserted could result in damage to the vocal cords or the trachea. This could lead to serious injuries, or death.
https://www.fcc.gov/fcc-bin/bye?https://www.weitzlux.com/firm-news/cortrak2-enteral-access-system/ According to Avanos Safety Communication the company has reported 60 injuries and 23 deaths related to this issue. feeding tube placement There were a variety of adverse events, including pneumothorax, respiratory failure, perforation as well as pleural effusion and pneumonia.
This recall is utilized to modify Cortrak*2's guidelines on use, intended use and also instruct users to confirm tube placement as per institutional guidelines prior to making use of the tube to provide nutritional benefits.
Clinicians were instructed to add the pertinent field correction notice in the operating manual. They must also return the acknowledgement form that came along with the Avanos notification. https://divulgaaqui.online/author/avanos-mediacal-cortrak-2jvga747/ Avanos Mediacal Cortrak 2 The users will shortly receive an update to the labeling and confirmation that the tubes were placed according to institution policy.
Website: https://www.transtats.bts.gov/exit.asp?url=https://www.nsmedicaldevices.com/news/avanos-medical-cortrak-2-eas-class-i-recall/
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