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FDA's Deadliest Recalls 2022 The Misplaced Feeding Tubes Ahead (Avanos Medical)
According to FDA recalls The Avanos Medical Cortrak2 feeding tube is among the top deadliest medical device.

Even though 2022 isn't over but the FDA has already compiled the list of 50 recalls for medical devices. The recalls have caused 36 deaths and more than 224 injuries. Avanos Medical is first on the list of 2022 for malfunctions in medical devices, with 23 reports of deaths due to misplaced feeding tubes.


These are the four deadliest medical device malfunctions as per the FDA medical device recall Notice:

Avanos Medical Recalls Cortrak*2 Enteral Access System to feed tubes
The misplacement of the nasogastric feed tube resulted in 60 injuries, and 23 fatalities.

Avanos Medical feeding tube This malfunctioning device is the most significant cause of death for all medical devices that were recalled by the FDA in 2022.


Avanos Medical feeding tube Avanos Medical has pulled the Cortrak*2 Enteral Access System from service due to injuries and deaths resulting from improper placement of nasogastric feeding tubes.


If a nasogastric or nasal, or nasoenteric, tube has been incorrectly placed, patients may suffer damage to the vocal cords, their lungs, or the trachea. This could result in serious injuries and even death. Avanos Medical notified that patients "...as well as hospitals should confirm the placement of N/NI tubes according hospital protocol. Cortrak 2 eternal access system Fox News covered the story.

Avanos Medical reported in a recall notice that fatalities and injuries were caused by misplacement or misuse of the enteral feeding tube while using the CORTRAK*2 Ental Access System.

Baxter recalls SIGMA Spectrum Infusion Pumps that have Master Drug Library (Version 8) and Spectrum IQ Infusion Systems with Dose IQ Safety Software (Version 9)
Baxter received 51 serious injuries as well as three reports of patient deaths in the past five years.

Baxter, a maker of medical devices and medical devices, has recalled the device following numerous reports of a malfunctioning safety alarm. The alarms on the pumps were not being activated in case of upstream occlusion events. The warnings were issued that these products could result in adverse health effects , and possibly even death.

Medtronic Recalls NIM Contact Reinforced EMG Endotracheal Tube
The device has been linked to 3 deaths and 2 injuries.

The NIM CONTACT Reinforced EMG Endotracheal Tube as well as the NIM Standard Reinforced EMG Endotracheal Tube - which are used to provide an airway as well as monitor laryngeal nerves during head or neck surgeries - were the source of three accidents and two deaths in the lead up to Medtronic's recall. Although the company hasn't asked customers to return defective products or replace them, they sent safety notices to ensure that the silicone cuff did not restrict a patient's airway.


Patients can suffer from an oxygen deficiency, brain injury or even death , if the tube is not properly ventilated.

Baxter Healthcare Corporation Recalls Volara System
There has been 1 death and 1 injury by the use of this device.

Baxter Healthcare Corporation and its subsidiary company Hillrom are recalling the Volara System due to the fact that an in-line ventilation adapter may hinder patients using home oxygen in getting enough oxygen from their ventilators. Avanos Medical The risk for patients affected include choking on mucus or other airway fluids, lung infections (pneumonia) that prevents oxygen from reaching the bloodstream (respiratory failure) and brain injuries caused by a lack in oxygen to the brain (hypoxia), and death.


This is the list of human deaths in 2022 due to medical device malfunctions or misuse.


Avanos Medical feeding tube https://www.fiercebiotech.com/medtech/avanos-medical-faces-class-i-recall-feeding-tube-system-linked-23-deaths-2015 Avanos Medical Recalls Cortrak*2 Enteral Access System

Injuries: 60

Deaths: 23

Baxter recalls SIGMA Spectrum Infusion Pumps that come with Master Drug Library (Version 8) and Spectrum IQ Infusion Systems With Dose IQ Safety Software(Version 9) the occlusions

Injuries: 51

Deaths: 3

Medtronic Recalls NIM CONTACT Reinforced Endotracheal Tube and the NIM Standard Reinforced EMG Endotracheal Tube

Injuries: 3

Deaths: 2

Baxter Healthcare Corporation Recalls Volara System

Injuries: 1

Deaths: 2

Smiths Medical Remands Certain Medfusion 3500 and 4000 Syringe Pumps

Injuries: 7

Deaths: 1

Medtronic recalls the HeartWare HVAD Systems Batteries

Injuries: 6

Deaths: 1

Philips Respironics Recalls All V60 and V60 Plus Ventilators

Injuries: 4

Deaths: 1

Medtronic Recalls the HVAD Pump Implant Kit

Injuries: 2

Deaths: 1

Medtronic Recalls the HVAD Systems HeartWare Batteries

Injuries: 0

Deaths: 1

Covidien, LP Recalls Puritan Bennett 980 Series Ventilator

Injuries: 0

Deaths: 1

Medtronic Inc. Recall of the HawkOne Directional Atherectomy Systems

Injuries: 55

Deaths: 0

Arrow International, LLC is a Subsidiary of Teleflex Inc., Recalls the Arrow Trarotola Percutaneous Thorolytic Device

Injuries: 14

Deaths: 0

Atrium Medical Corporation Recalls iCast Covered Stent

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 the SafeStar55 Breathing System 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


Homepage: https://www.fiercebiotech.com/medtech/avanos-medical-faces-class-i-recall-feeding-tube-system-linked-23-deaths-2015