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Avanos Recalls Cortrak*2 Over Potential Enteral Tube Misplacement
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 type. https://www.inventables.com/users/choatelivingston3118 Avanos Medical feeding tube These devices can cause serious injuries, or even death.

feeding tube placement Sam Brusco Associates Editor05.16.22

The FDA has confirmed Avanos Medical’s recall of its Cortrak*2 intramuscular accessibility system. Since March 21st, 2016, 629 devices were recalled in the U.S.

Cortrak*2 helps clinicians place medical feeding tubes in the stomach or in the small bowels of patients who require nutrition through the tube.

Avanos Mediacal Cortrak 2 The recall was initiated in response to reports of injuries and deaths in patients due to misplacement of nasocentric or gastric tubes. The device is used to place the tubes. A mistake in the placement of the Nasogastric or Nasoenteric tube could cause severe injuries or even death.

According to Avanos Safety Communication There have been 60 injuries and 23 deaths related to this issue. Some of the adverse events reported were pneumothorax, respiratory failure perforation, pneumonia, and the development of pleural effusion.

Cortrak*2 will make use of the recall to revise its instructions for usage and intended usage. It will advise users to verify tube placement using institutional protocols before delivering food.

Clinicians are also advised to include the field correction notice to the operating guideline and return the acknowledgement forms included in the notice to Avanos. feeding tube placement The company hopes to soon give users with an updated labeling. This includes confirmation that the placement of the tube was carried out in accordance with institutional guidelines.


Homepage: https://www.inventables.com/users/choatelivingston3118
     
 
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