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This problem has been the cause for the deaths of 60 and 23 injuries.
The FDA has designated this as a Class I Recall, which is the most serious kind. Avanos Medical Use of these devices may result in 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 enteral access. Since March 21st in 2016, 629 of the devices were recalled in the U.S.
Avanos Medical feeding tube Cortrak*2 is a device that allows doctors to place medical feeding tubes inside patients stomachs or small bowels.
The device was temporarily recalled due to injury and patient death reports following nasocentric or Nasogastric tube misplacement, when it is employed to help place these tubes. Nasogastric, also known as nasal, tube that isn't properly inserted could result in damage to the vocal cords or trachea. This could lead to severe injury or death.
https://list.ly/wilderknight971 According to Avanos’ safety communication, there were 60 deaths and 23 injuries that were related to the issue. https://www.princeclassified.com/user/profile/1009170 There have been several adverse events, including pneumothorax, respiratory failure, perforation, pneumonia and pleural effusion.
This recall is utilized to modify Cortrak*2's guidelines regarding use, intended usage, and advise users to confirm tube placement as per institutional guidelines prior to using the tube to deliver nutrition.
Clinicians are also advised to attach the field correction notice to the operating manual and return the acknowledgement forms included with the notice to Avanos. The company will soon be able provide the latest labels to patients, as well as confirmation of the placement of tubes as per institutional policies.
Avanos Mediacal Cortrak 2
Here's my website: http://pandora.nla.gov.au/external.html?link=https://www.openlearning.com/u/bredahlgram-rkwzge/blog/FdaHasIdentifiedAvanosSCortrak2EasRecallAsClassI
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