This has resulted in 60 injuries, and 23 deaths. https://marketbusinessnews.com/cortrak-avanos-medical-nim-standard-deadly-feeding-tube-recalls/324830/ This recall has been classified by FDA as a class I recall. This is the most serious type. These devices could cause serious injuries or even death. Sam Brusco is Associate Editor05.16.22 The FDA has identified Avanos Medical as the one responsible for recalling its Cortrak*2 system of access to the enteral. The recall of 629 devices that were distributed between 2016 and 2022 started on March 21. Cortrak*2 is a device that permits doctors to place medical feeding tubes inside patients' stomachs or small bowels. The recall was caused by reports of death and injuries from patients who suffered from nasocentric or nasogastric mistaken placement. This device is utilized to aid in the placement of the tubes. Avanos Medical feeding tube When you are not careful, inserting a nasogastric tube or nasoenteric one can cause severe injury, or even death. Avanos Medical feeding tube According to Avanos' safety communications there were 60 injuries and 23 deaths related to this issue. Cortrak 2 eternal access system Pneumothorax (perforation), pneumothorax (perforation) and pneumonia and pleural effusion were all listed as adverse events. https://www.justice.gov/opa/pr/avanos-medical-inc-pay-22-million-resolve-criminal-charge-related-fraudulent-misbranding-its Cortrak*2 will use this recall to update the instructions for its the use and intended usage. Cortrak 2 eternal access system Avanos Medical The users will have to confirm the proper placement of tubes in accordance with established protocols before they are able to deliver nutritional supplements. Clinicians were also advised to attach the field-correction notice to the operating manual , and return the acknowledgement form included in the notice to Avanos. Users will soon receive updated labeling and confirmation that tubes were placed according to institution policies. Avanos Medical feeding tube
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