Notes

The most deadly FDA Recalls 2022. - Lost Feeding Tubes The most feared (Avanos Medical)
Avanos Medical Cortrak2 feeding tubes are among the most deadly medical devices as per FDA recalls.

Although 2022 is still not completed, the FDA has already prepared the following list of recalls of medical devices. https://profiteplo.com/user/Avanos.Mediacal.Cortrak.2igko742/ The impact of these recalls as of now is a sad 36 deaths and more than 224 injuries. Avanos Medical ranks first on the list of 2022 medical device failures with 23 deaths reported due to misplaced feeding tubes.


These are the most risky medical device mistakes in accordance with the FDA recall notice:

Avanos Medical Recalls Cortrak*2 Ental Access System for Feeding Tubes
The improper placement of nasogastric tube feeding caused more than 23 deaths and 60 injuries.

This is the most frequent cause of death in recalled devices.


Avanos Medical has pulled the Cortrak*2 Enteral Access System from service because of accidents and deaths that result from inadvertently placing nasogastric feed tubes.


If a nasal nasogastric nasoenteric, tube is incorrectly put in the wrong place, patients can be harmed by the vocal cords, their lungs, or the trachea. https://independent.academia.edu/HalbergSherwood2 This can cause serious injury , and possibly death. Avanos Medical notified that patients "...and hospitals should verify the positioning of the N/NI tubes as per institutional guidelines. Fox News covered the story.

Avanos Medical reported in a recall notification that deaths and injuries were caused by the improper placement or the use of an feed tubes to the stomach while employing the CORTRAK*2 Ental Access Systems.

https://www.metooo.io/u/6457e92ef6be933d0474e96d Avanos Medical Baxter recalls SIGMA Spectrum Infusion pumps that have Master Drug Library (Version 8) and Spectrum IQ Infusion Systems With Dose IQ Safety (Version 9)
Baxter has received 51 complaints of serious injuries as well as three deaths of patients over five years potentially associated with this problem.

The medical device manufacturer Baxter recalled this device after numerous reports of a security alarm malfunction. The alarms on the pumps were not being activated in case of upstream occlusions. The announcement warned that the use of these affected products could result in adverse health effects, including death.

Medtronic Recalls the NIMCACT Reinforced Endotracheal Tube EMG
This device has been associated with 3 injuries and 2 fatalities.

The NIM CONTACT Reinforced EMG Endotracheal Tube and the NIM Standard Reinforced EMG Endotracheal Tube - which are utilized to create an airway as well as monitor laryngeal nerves undergoing head and neck surgery - are the source of three accidents and two deaths ahead of Medtronic's recall. Although Medtronic isn't asking for its customers to return their damaged devices, it has sent out safety alerts to help prevent the silicone cuff to block a patient's airway.


Cortrak 2 eternal access system Patients may suffer from cerebral damage, oxygen deprivation or death when the tube isn't ventilated well or block airways.

Baxter Healthcare Corporation Recalls Volara System
There was one incident of injury and 2 deaths by the use of this device.

Baxter Healthcare Corporation and its subsidiary company Hillrom are recalling the Volara System due to the fact that the in-line ventilator adapter could prevent patients who use home care from getting enough oxygen from their ventilators. There are risks for patients affected such as choking on mucus and other airway secretions, lung infection (pneumonia) that blocks oxygen from getting into the blood (respiratory failure), brain injury due to a lack in oxygen (hypoxia) and along with death.


This is the list of human lives lost in 2022 due malfunctioning medical devices or improper use.


Avanos Medical Remcalls Cortrak*2 Entry Access System

Injuries: 60

Deaths: 23

Baxter recalls SIGMA Spectrum Infusion Pumps equipped with Master Drug Library (Version 8) and Spectrum IQ Infusion Systems with Dose IQ Safety Software (Version 9) Occlusion events

Injuries: 51

Deaths: 3

Medtronic recalls NIM CONTACT Reinforced Endotracheal Tube and the NIM Standards Reinforced-EMG Endotracheal Tube

Injuries: 3

Deaths: 2

Baxter Healthcare Corporation Recalls Volara System

Injuries: 1

Deaths: 2

Smiths Medical Recalls Certain Medfusion 3500 and 4000 Syringe Infusion Pumps

Injuries: 7

Deaths: 1

Medtronic recalls the HeartWare HVAD system batteries

Injuries: 6

Deaths: 1

Philips Respironics Recalls All V60 Ventilators

Injuries: 4

Deaths: 1

Medtronic Recalls HVAD Pump Kit

Injuries: 2

Deaths: 1

Medtronic recalls batteries of the HeartWare HVAD system

Injuries: 0

Deaths: 1

Covidien, LP Recalls Puritan Bennett 980 Series Ventilator

Injuries: 0

Deaths: 1

Medtronic Inc. https://peatix.com/user/17207385 Recalls HawkOne Directional Atherectomy System

Injuries: 55

Deaths: 0

Arrow International, LLC, Subsidiary to Teleflex Inc., Recalls the Arrow Trarotola Percutaneous Thorolytic Device

Injuries: 14

Deaths: 0

Atrium Medical Corporation recalls iCast covered sten

Injuries: 9

Deaths: 0

Vyaire Medical Recalls Bellavista1000e Series Ventilators

Injuries: 7

Deaths: 0

LivaNova (TandemLife) Recalls LifeSPARC System

Injuries: 2

Deaths: 0

Draeger, Inc recalls SafeStar 55 Breathing Systems Filters

Injuries: 1

Deaths: 0

Abbott Medical Recalls Dragonfly OpStar Imaging Catheter

Injuries: 1

Deaths: 0

SML Distribution LLC Recalls Skippack Medical Lab COVID-19 Direct Antigen Rapid Tests

Injuries: 1

Deaths: 0

feeding tube placement
Here's my website: http://spectr-sb116.ru/user/Avanos.Mediacal.Cortrak.2orwc302/