Notes

The most deadly FDA Recalls 2022. - Lost Feeding Tubes Inspiring (Avanos Medical)
Based on FDA recalls The Avanos medical Cortrak2 feeding tube is the top deadliest medical device.

Avanos Medical feeding tube Although 2022 is still not finished even though 2022 isn't over yet, the FDA has already put together an inventory of 50 recalls of medical devices. The recalls have led to 36 deaths and 228 injuries. Avanos Medical Avanos Medical is first on the 2022 list for malfunctions of medical devices, and has 23 reported deaths due to misplaced feeding tubes.


The four most deadly medical device malfunctions as per the FDA medical device recall Notice:

Avanos Medical Recalls Cortrak*2 Enteral Access System for feeding tubes
Misplacement of nasogastric feed tubes resulted in 60 injuries, and 23 deaths.

Avanos Medical This is the most frequent cause of death among recalled devices.


Avanos Medical has recalled the Cortrak*2 Enteral Access System due to reports of injuries and deaths resulting from nasoenteric and nasogastric feeding tubes were placed incorrectly.


Avanos Medical If a nasogastric, also known as a nasoenteric, tube is incorrectly placed, patients could suffer damage to the vocal cords, their lungs, or trachea. This can cause serious injury , and possibly death. Avanos Medical issued a notification to patients requesting that they confirm the positioning of the NG/NI tubing according to hospital protocol. Fox news announced.

Avanos Medical's recall communications reported that the CORTRAK*2 Enteral Access System has been misplaced enteral feeding tubes since the year 2015.

Baxter recalls SIGMA Spectrum Infusion Systems that include Master Drug Library (Version 8) and Spectrum IQ Infusion Systems (Version 9)
Baxter received 51 cases of serious injury and three reports on patients' deaths over the last five years.

After numerous complaints of safety alarm malfunctions The medical device maker Baxter has announced a recall of the device. The alarm on the pumps was failing to sound in the event of upstream occlusion events. It was warned that the products could result in adverse health effects and even death.

Medtronic recalls NIM CONTACT Reinforced EMG Endotracheal Tube
The device has been associated with three injuries and two deaths.

Three injuries and two deaths were caused by the NIMCONTACT Reinforced EMG Endeotracheal Tube and NIM Standard Reinforced EMG Endotracheal Tube both of which serve to monitor laryngeal and head nerves. Avanos Medical Cortrak 2 eternal access system While Medtronic hasn't asked clients to return the damaged devices, the company issued safety warnings in order to prevent the cuff made of silicone from blocking the airway of a patient.


If the tube does not adequately ventilate or block the airway, patients may suffer from deprivation of oxygen or brain damage. This could lead to death.

Baxter Healthcare Corporation Recalls Volara System
The device has been linked with one injury and two deaths.

Avanos Medical feeding tube Baxter Healthcare Corporation, and Hillrom its subsidiary company, are recalling its Volara Systems. This is due to the fact that the adaptor for in-line ventilators may not allow patients with home use to get enough oxygen. There is a risk for the patients which include choking upon mucus as well as other airway secretions and lung infection (pneumonia) that blocks oxygen from getting into the bloodstream (respiratory failure) and brain injuries due to a lack in oxygen (hypoxia) as well as death.


This list contains people's lives that were lost due to the misuse of medical devices or their malfunction in 2022.


Cortrak 2 eternal access system Cortrak 2 eternal access system Avanos Medical Remcalls Cortrak*2 Entry 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-related events

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 Recalls Certain Medfusion 3500 and 4000 Syringe Pumps

Injuries: 7

Deaths: 1

Medtronic recalls HVAD HeartWare system batteries

Injuries: 6

Deaths: 1

Philips Respironics recalls all V60 and V60 Plus ventilatilators

Injuries: 4

Deaths: 1

Medtronic recalls the HVAD Pump Implant Kit

Injuries: 2

Deaths: 1

Medtronic Recalls HeartWare HVAD System 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-Trerotola PercutaneousThrombolytic Device

Injuries: 14

Deaths: 0

Atrium Medical Corporation Recalls the iCast-Covered Stent

Injuries: 9

Deaths: 0

Vyaire Medical Recalls Bellavista 1000 Series and 1000e Series Ventilators

Injuries: 7

Deaths: 0

LivaNova (TandemLife) Recalls LifeSPARC System

Injuries: 2

Deaths: 0

Draeger, Inc Recalls 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


Here's my website: https://www.rheingoldlaw.com/blog/2022/may/avanos-faces-fda-class-i-recall-after-23-deaths-/