Notes

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

Avanos Medical feeding tube https://dohabb.com/index.php?page=user&action=pub_profile&id=1943986 Although 2022 isn't yet completed, FDA already has 50 medical devices on its recall list. This recall has resulted in the tragic deaths of 36 and 228 injuries. Avanos Medical ranks number one on the 2022 medical device malfunctions list with 23 deaths reported from the wrong placement of the feeding tube.


These are the 4 deadliest medical device malfunctions , according to the FDA medical device recall notice:

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

This is the most common cause of death for recalled devices.


Avanos Medical has pulled the Cortrak*2 Enteral Access System from service due to accidents and deaths that result from incorrect placement of nasogastric feed tubes.


Patients may suffer serious injuries or even death if the nasogastric tube or nasoenteric tub has been improperly placed. Avanos Medical issued a note to patients requesting that they confirm the placements of the NG/NI tube according to institutional procedure. https://www.indiegogo.com/individuals/31189330/ Fox news reported.

Avanos Medical's recall notification reported the injuries and deaths caused by the misplacement of the feeding tubes for the enteral system during the use of the CORTRAK* 2 Enteral Access System since 2015.

Baxter recalls SIGMA Spectrum Infusion Systems with Master Drug Library (Version 8) and Spectrum IQ Infusion Systems (Version 9)
Baxter has received 51 reports of serious injuries, and three reports of patient deaths over five years potentially associated with this issue.

Baxter, a maker of medical devices has announced a recall of the device following numerous reports of a failure in the safety alarm. The alarm on the pumps failed to trigger in the event of upstream occlusion events. The announcement warned that use of the affected products could cause adverse health effects, which could lead to death.

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

Three injuries and two deaths resulted from the NIMCONTACT Reinforced EMG Endotracheal Tube and NIM Standard Reinforced EMG Endotracheal Tube that serve to monitor the head and laryngeal nerves. While the company does not ask customers to return defective products or replace the devices, they did send out security alerts to ensure the cuff's silicone material didn't restrict a patient's airway.


Avanos Mediacal Cortrak 2 Patients can suffer from oxygen deprivation, brain damage or death when the tube isn't ventilated well or blocks the airway.

Baxter Healthcare Corporation Recalls Volara System
There has been 1 accident and 2 deaths that have been linked by the use of this device.

Baxter Healthcare Corporation is recalling its Volara system subsidiary, Hillrom. The adaptor in-line to ventilators could prevent patients at-home from getting enough oxygen. The most vulnerable patients are those who breath in mucus and respiratory failure (pneumonia) as well as brain injury (hypoxia), and coughing.


Here is the list of the human life paid in 2022 for mishaps with medical devices or improper use:


Avanos Medical Remcalls Cortrak*2 Entry Access System

Injuries: 60

Deaths: 23

Baxter recalls SIGMA Spectrum Infusion Pumps (Version 8) and Spectrum IQ Infusion Systems (Version 9) Occlusions

Injuries: 51

Deaths: 3

Medtronic recalls NIMCONTACT Reinforced Endotracheal Tube with EMG Reinforcement as well as the NIM Standard Reinforced 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 HVAD Systems HeartWare 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 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, Subsidiary of Teleflex Inc., recalls the Arrow-Trerotola PercutaneousThrombolytic Device

Injuries: 14

Deaths: 0

Atrium Medical Corporation Recalls ICast, a Stent that is covered by the iCa

Injuries: 9

Deaths: 0

Vyaire Medical Recalls Bellavista 1000 and 1000e Series Ventilators

Injuries: 7

Deaths: 0

LivaNova (TandemLife) Recalls LifeSPARC System

Injuries: 2

Deaths: 0

Draeger, Inc Recalls SafeStar 55 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

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