Medtronic Recalls Certain Newport Ventilators
The FDA has designated Medtronic's voluntary recall notification for specific Newport HT70 and HT70 Plus ventilators and certain related Newport service parts as a Class I recall.
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Medtronic Recalls Certain Newport Ventilators
The FDA has designated Medtronic’s voluntary recall notification for specific Newport HT70 and HT70 Plus ventilators and certain related Newport service parts as a Class I recall.
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Medtronic Recalls Shiley Tracheostomy Tube
Medtronic is recalling its Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula as the tube may become dislodged or move out of place if the securement flange becomes disconnected, according to the FDA.
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Experts Call for Shift to Video Laryngoscopy as New Gold Standard
Recent trials demonstrate higher first-pass intubation success rates with video laryngoscopy compared to direct laryngoscopy, prompting calls for widespread adoption.
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Medtronic Launches VitalFlow ECMO System
Medtronic has launched a new ECMO system called VitalFlow, which is designed to provide extracorporeal life support between bedside care and intrahospital transport, according to the company.
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Medtronic Removes Certain McGrath MAC Video Laryngoscopes
The company is also updating use instructions for another video laryngoscope due to an increased risk of battery overheating and explosion.
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FDA: Do Not Use Certain Medtronic Endotracheal Tubes
Medtronic has recalled specific endotracheal tubes after receiving complaints about blockages leading to serious health risks, prompting an FDA alert to health care providers.
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SonarMed Recalls Airway Sensors Due Failure to Detect Partial Obstructions
The recall of the sensors, used in conjunction with the SonarMed airway monitoring system, is due to a restricted inner diameter that impedes the passage of suction catheters.
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Medtronic Updates Recommendations for Airway Obstruction Risk in Certain Endotracheal Tubes
Medtronic issued updated recommendations for the potential risk of airway obstruction in its NIM CONTACT Reinforced EMG Endotracheal Tube and NIM Standard Reinforced EMG Endotracheal Tube, according to an FDA alert.
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Medtronic to Discontinue Puritan Bennett Ventilators, Exit Ventilator Business
Medtronic will discontinue its Puritan Bennett ventilator series, including the Puritan Bennett 980, Puritan Bennett 840, and Puritan Bennett 560 ventilators.
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Enhancing Patient Care in Assisted Ventilation: A Closer Look at Patient-Ventilator Synchrony
Discover groundbreaking strategies in our white paper on patient-ventilator synchrony. Authored by Cyndy Miller of Medtronic, this essential read highlights the Puritan Bennett™ 980 ventilator and IE Sync™ software, offering innovative solutions to enhance patient outcomes in assisted ventilation. Ideal for respiratory therapists and doctors seeking advanced knowledge in ICU patient care.
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Medtronic Recalls McGrath MAC Video Laryngoscopes
Medtronic-owned Covidien LLC is recalling the McGrath MAC Video Laryngoscope in order to remove stolen defective models that have been offered for sale illegally by unauthorized third parties, according to an FDA alert.
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Medtronic Warns of Defective Laryngoscopes Being Sold Illegally
Medtronic issued a notification to inform the public of stolen defective video laryngoscopes that have been offered for sale illegally by unauthorized third parties through social media platforms.
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Patient Safety at the Core of Ventilator Care in the ICU
Introducing the Puritan Bennett™ PB980: the future of ICU ventilation. Redefining safety and efficiency, it’s a game-changer for respiratory care. Delve deeper with our white paper.
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Is a Lateral Suction Port Effective in Subglottic Tracheostomy Tubes?
Researchers tested the secretion clearing effectiveness of Medtronic’s new subglottic tracheostomy tube equipped with a lateral suction port.
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Medtronic to Spin off its Patient Monitoring and Respiratory Interventions Businesses
Medtronic says it will pursue a separation of the company’s combined patient monitoring and respiratory interventions businesses.
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FDA Issued Guidance on the Medtronic Electromyogram Endotracheal Tube Recall
The FDA issued guidance on the Medtronic electromyogram endotracheal tube recall after the company announced the risk of airway obstruction.
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Medtronic to Exclusively Distribute BioButton Continuous Remote Patient Monitor in US
Medtronic plc has entered into a strategic partnership with BioIntelliSense for the exclusive US hospital and 30-day post-acute hospital to home distribution rights of the BioButton multi-parameter wearable for continuous, connected monitoring.
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GE Healthcare Integrates Medtronic Capnography, Oximetry into Carescape Monitoring
GE Healthcare has integrated Medtronic Microstream capnography and INVOS regional oximetry technology into its Carescape precision monitoring platform for perioperative and ICU care.
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Medtronic Completes Acquisition of Intersect ENT
Medtronic plc has completed the acquisition of Intersect ENT, expanding the company’s comprehensive ear, nose, and throat (ENT) portfolio with products used in sinus procedures to improve post-operative outcomes and to treat nasal polyps.
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FDA Clears Medtronic Nellcor OxySoft Neonatal-Adult SpO2 Sensor
The Medtronic Nellcor OxySoft Neonatal-Adult SpO2 Sensor is the first pulse oximetry sensor with silicone adhesive designed to protect fragile newborn skin while staying adhered longer.
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Medtronic, GE Healthcare Collaborate on Outpatient Care
Medtronic and GE Healthcare are collaborating to provide solutions and services to Ambulatory Surgery Centers and Office Based Labs.
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Medtronic, GE Healthcare Collaborate on Outpatient Care
Medtronic and GE Healthcare will collaborate to provide greater access to the companies’ product portfolios, financial solutions, and services at Ambulatory Surgery Centers and Office Based Labs.
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Medtronic Appoints New Chief Scientific Officer
Medtronic plc has appointed Laura Mauri, MD, MSc, as its chief Scientific, Medical and Regulatory officer.
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Medtronic RespArray Patient Monitor Cleared by FDA
Medtronic plc received US FDA 510(k) clearance for its RespArray patient monitor, designed for procedural sedation and medical-surgical units.
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