Notes

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

https://www.medtechdive.com/news/avanos-medical-recall-class-i/623892/ Even though 2022 isn't over even though 2022 isn't over yet, the FDA has already put together the list of 50 recalls for medical devices. This recall resulted in the tragic deaths of 36 and 224 injuries. Avanos Medical https://www.medicaldevice-network.com/news/fda-avanos-medical-cortrak2-eas-recall/ Avanos Medical is first on the list of 2022 for malfunctions of medical devices, and has 23 reported deaths due to misplaced feeding tubes.


The four are the most serious medical device malfunctions, according to the FDA recall notice.

Avanos Medical Recalls Cortrak*2 Ental Access System for Feeding Tubes
Inadvertently, removing nasogastric feeding tubes caused 60 injuries and 23 deaths.

It is the most frequently reported reason for death in recalls of devices.


Cortrak 2 eternal access system Avanos Medical has recall the Cortrak*2 Enteral Access System after reports of deaths and injuries among patients who had nasogastric or nasoenteric feeding tubes that were not correctly placed.


Patients are at risk of serious injury or even death if a nasogastric tub or nasoenteric one is wrongly inserted. Avanos Medical notified that patients "...and hospitals must confirm the location of N/NI tubes in accordance with institutional guidelines. Avanos Medical feeding tube Fox News reported.

Avanos Medical's recall announcement included the fatalities and injuries caused by the misplacement of the tubes feeding into the enteral lining when using the CORTRAK* 2 Enteral Access System since 2015.

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)
Baxter has received 51 complaints of serious injuries, and three deaths reported by patients over the course of five years, which could be linked with this problem.

After numerous complaints of safety alarm malfunctions after numerous complaints of safety alarm malfunctions, the medical device maker Baxter has decided to recall this device. If there was an obstruction in the upstream the alarm was unable to start the pumps. Avanos Medical feeding tube It was warned that the products could result in adverse health consequences and may even lead to death.

Medtronic Recalls EMG Reinforced Endotracheal Tube
The device has been associated with 2 deaths and 3 injuries.

The NIMCONTACT Reinforced EMG Tube and the NIM Standard Reinforced EMG Tube Both utilized to supply airway and monitor laryngeal nervous systems during neck and head surgeries was responsible for two deaths and three injuries before Medtronic's recall. Even though Medtronic hasn't requested its customers to return their defective devices, the company sent out safety alerts in order to prevent the cuff made of silicone from blocking the airway of a patient.


If the tube does not effectively ventilate or blocks the airway, patients may be afflicted with oxygen deprivation as well as brain damage, and even death.

Baxter Healthcare Corporation Recalls Volara System
The usage of this device has led to 1 injury, 2 deaths.

Baxter Healthcare Corporation, and Hillrom its subsidiary company are recalling the Volara Systems. The reason for this is that the adaptor that is used to connect in-line ventilators may not allow home-use patients to get enough oxygen. The risk for patients affected are choking on mucus, or other airway secretions lung infections (pneumonia) that prevents oxygen from reaching the blood (respiratory failure) as well as brain injury due to a lack of oxygenation to the brain (hypoxia) and even death.


This is a list of people's lives that were lost because of medical device failure or misuse in 2022.


Avanos Medical Recalls Cortrak*2 Enteral Access System

Injuries: 60

Deaths: 23

Baxter recalls SIGMA Spectrum Infusion Pumps 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 EMG 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 Recalls Certain Medfusion 3500 and 4000 Syringe Infusion Pumps

Injuries: 7

Deaths: 1

Medtronic Recalls HeartWare HVAD System Batteries

Injuries: 6

Deaths: 1

Philips Respironics Recalls All V60 Ventilators

Injuries: 4

Deaths: 1

Medtronic recalls the HVAD Pump Implant Kit

Injuries: 2

Deaths: 1

Medtronic recalls the HeartWare HVAD Systems Batteries

Injuries: 0

Deaths: 1

Covidien, LP Recalls Puritan Bennett 980 Series Ventilator

Injuries: 0

Deaths: 1

Medtronic Inc. Recall of HawkOne Directional Atherectomy Systems

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 Stents Covered

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

Cortrak 2 eternal access system
Read More: https://aacnjournals.org/ajcconline/article/26/2/149/3230/Cortrak-Assisted-Feeding-Tube-Insertion-A