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Avanos Medical recalled Cortrak* 2 EAS in the wake of incidents of injury and patient deaths due to tube misplacements.
Avanos Medical The US Food and Drug Administration has classified Avanos Medical’s Cortrak*2 Enteral Access System (EAS), as a Class 1 recall.
A Class I remember is the most serious one of the three classes.
Avanos Medical has recalled Cortrak*2 EAS due to reports of injuries or deaths from nasogastric tube misplacements.
The device is intended to help health care workers to place medical feeding tubes on patients.
But, incorrect placement of the nasogastric/nasoenteric tubs result in severe injuries or even death.
Avanos Medical The recall affects 629 devices that were available in the US between 1 February 2016 and 1 January 2022.
Avanos Medical The company also said in a recall announcement that there were 60 injuries and 23 patients who died since 2015 due to the incorrect placement of nasogastric feed tubes when using the Cortrak* 2 EAS.
Avanos Medical is updating the marking on the device following the recall. This will include updated instructions on how to use the device and the intended use of the Cortrak*2 EAS.
Users are also directed to confirm that the tubes have been put in the correct manner according to the guidelines of the institution before they make use of them.
Avanos Medical has its headquarters in Alpharetta Georgia. feeding tube placement Avanos Medical markets its well-known brands across more than 90 countries.
Avanos Medical feeding tube https://myclc.clcillinois.edu/web/jeff_test/ttttttutoring/-/message_boards/message/38694049 The company signed a $160 million contract in December last year to purchase OrthogenRx. Avanos Medical closed on the acquisition in January.
Homepage: http://sc.sie.gov.hk/TuniS/controlc.com/2e5c2a9f
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