According to FDA recalls The Avanos medical Cortrak2 feeding tube is the highest-risk medical device. Although 2022 isn't yet completed, FDA already has 50 medical devices listed on the recall list. Cortrak 2 eternal access system The effect of these recalls thus far is a sad 36 deaths and 224 injuries. Avanos Medical is first on the 2022 list for malfunctions in medical devices, with 23 reports of deaths due to the wrong placement of feeding tubes. They are the four most dangerous medical device malfunctions according to the FDA recall notice. Avanos Medical Recalls Cortrak*2 Enteral Access System to feed tubes The improper placement of feeding tubes led to sixty injuries and 23 deaths. In 2022 the year 2022, the malfunction of this device was the primary cause of death in all recalls of medical equipment. Avanos Medical has pulled the Cortrak*2 Enteral Access System from service because of injuries and deaths resulting from inadvertently placing nasogastric feed tubes. Cortrak 2 eternal access system Patients could be seriously injured or even death if the nasogastric tube or nasoenteric tub is wrongly placed. In order to protect themselves, Avanos Medical sent warning to doctors, suggesting that the patient or the hospital ...confirm the location of the NG/NI tube according to hospital guidelines Fox news reported. Avanos Medical Avanos Medical feeding tube Avanos Medical's recall notification disclosed the deaths and injuries related to the misplacement of the feed tubes to the stomach during the use of the CORTRAK* 2 Enteral Access System since 2015. Baxter recalls SIGMA Spectrum Infusion Systems, which includes Master Drug Library (Version 8) & Spectrum IQ Infusion Systems (Version 9) Baxter received 51 complaints of serious injuries as well as three reports of patient deaths within the last five years. Avanos Medical feeding tube The medical device manufacturer Baxter recalled this device after numerous reports of a safety alarm malfunction. The alarm on the pumps failed to sound in the event of occlusions in the upstream. The announcement warned that use of these products can cause adverse health effects, which could lead to death. Cortrak 2 eternal access system Medtronic recalls NIM CONTACT Reinforced EMG Endotracheal Tube The device's use resulted in 3 injuries as well as 2 deaths. The NIM CONTACT Reinforced EMG Endotracheal Tube and the NIM Standard Reinforced EMG Endotracheal Tube that are used to open an airway and to monitor the laryngeal nerves in head and neck surgery - are the cause of three injuries and two deaths in the lead up to Medtronic's recall. Although the company hasn't asked customers to return defective devices or to replace the devices, they did send out warnings about safety to make sure that the silicone cuff did not impair a patient's airway. Patients can be affected by the lack of oxygen, brain damage or even death when the tube does not ventilate well or block airways. Baxter Healthcare Corporation Recalls Volara System The application of this device led to 1 injury, 2 deaths. Baxter Healthcare Corporation is recalling its Volara system subsidiary, Hillrom. The adaptor on the line to ventilators can prevent home-use patients getting enough oxygen. The most vulnerable patients are breathing in mucus and respiratory failure (pneumonia) and brain injury (hypoxia), and coughing. Here is the list of the human life-saving costs in 2022 for mishaps with medical devices or improper use: Avanos Medical Recalls Cortrak*2 Ental 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 NIM CONTACT Reinforced-EMG 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 4000 and 3500 Syringe Infusion Pumps Injuries: 7 Deaths: 1 Medtronic recalls HeartWare HVAD System 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 HeartWare HVAD Systems Batteries Injuries: 0 Deaths: 1 Covidien, LP Recalls Puritan Bennett 980 Series Ventilator Injuries: 0 Deaths: 1 Medtronic Inc. Recalls HawkOne Directional Atherectomy System 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 iCast Covered Stent Injuries: 9 Deaths: 0 Vyaire Medical recalls bellavista1000 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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