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This problem has resulted in the deaths of 23 people and 60 injuries.
Cortrak 2 eternal access system The recall has been classed by FDA as a class I recall. This is the most serious form of recall. Cortrak 2 eternal access system https://www.nsmedicaldevices.com/news/avanos-medical-cortrak-2-eas-class-i-recall/ These devices could cause serious injuries and even death.
Cortrak 2 eternal access system Sam Brusco Associates Editor05.16.22
The FDA has identified Avanos Medical's recall of the Cortrak*2 useal access system. Cortrak 2 eternal access system Since March 21st in 2016, 629 of the devices were recalls in the U.S.
Cortrak*2 assists clinicians in placing medical feed tubes into patients who require nutrition via the tube.
The system was recalled because of injury and deaths resulting from nasocentric or Nasogastric tube misplacement, when the device is used to to insert these tubes. An incorrectly placed nasogastric/nasoenteric tube can cause serious injury or death.
According to Avanos the safety announcement, there have been 53 deaths and 60 injuries in connection with this incident. Cortrak 2 eternal access system Many adverse events have been reported such as respiratory failure, pneumonia, and pneumothorax.
Cortrak*2 is using this recall to update its instructions for the use and intended usage. The users will have to verify the location of the tubes according to institutional protocols, before they can deliver nutrition.
Clinicians were also encouraged to add the updated note in the field on the problem to Avanos operating manual and return the acknowledgement forms in Avanos' notice. Avanos plans to give users current labels, as well as confirmation of placement of tubes in accordance to institutional policies.
Read More: https://aacnjournals.org/ajcconline/article/26/2/149/3230/Cortrak-Assisted-Feeding-Tube-Insertion-A
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