FDA: Do Not Use Certain Medtronic Endotracheal TubesÂ
Medtronic has recalled specific endotracheal tubes after receiving complaints about blockages leading to serious health risks, prompting an FDA alert to health care providers.
Medtronic has recalled specific endotracheal tubes after receiving complaints about blockages leading to serious health risks, prompting an FDA alert to health care providers.
Medtronic has recalled specific endotracheal tubes after receiving complaints about blockages leading to serious health risks, prompting an FDA alert to health care providers.
Read MoreMedline issued the recall due to risk of the inflation tube or other components becoming detached or torn from the main tube.Â
Read MoreThe 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.
Read MoreMedline Industries announced the acquisition of the manufacturing rights and intellectual property of AG Cuffill from Hospitech Respiration Ltd.
Read MoreMedtronic 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.
Read MoreRecent product innovations in intubation and airway management offer respiratory therapists opportunities to optimize therapy and enhance patient outcomes.Â
Read MoreThrough the transaction, SunMed is adding the Ballard, Microcuff, and endOclear product lines to its portfolio.
Read MoreEndotracheal, nasotracheal, and tracheostomy tubes can provide a high level of support for critically ill patients—if effective management of these artificial airways is maintained.
Read MoreIn RT’s January-February 2023 issue, RTs offer 5 tips for measuring spirometry and 8 considerations for delivering oxygen therapy to COPD patients; airway clearance options for bronchiectasis; and cylinder-free solutions for nitric oxide delivery.
Read MoreEndotracheal suctioning is one of the most commonly performed NICU/PICU interventions but the practice requires special care for neonatal and pediatric airways.Â
Read MorePrematurity and immature development of the pulmonary system, severe illness, trauma, overdose, aspiration, and other cardiopulmonary conditions call for protection of the airway and establishment of a safe and secure means to ventilate.
Read MoreThe FDA issued guidance on the Medtronic electromyogram endotracheal tube recall after the company announced the risk of airway obstruction.
Read MoreDale Medical Products has introduced its new BreezeLock Endotracheal Tube Holder, featuring a soft, comfortable, flexible neckband with no hard plastic parts.
Read MoreThe FDA issued 510(k) clearance for GE Healthcare’s artificial intelligence algorithm to help clinicians assess endotracheal tube (ETT) placements.
Read MoreA coating applied to endotracheal tubes can release antimicrobial peptides that target infectious bacteria and reduce upper-airway bacterial inflammation during intubation.
Read MoreAirway management is an integral part of caring for critically ill patients receiving mechanical ventilation and the COVID-19 pandemic has brought on some changes and new considerations.
Read MoreB&B Medical Technologies’ Baby Tape Plus is a pre-cut endotracheal tube holder made from a non-irritating, latex free hydrocolloid adhesive that is skin friendly for infants.
Read MoreGE Healthcare announced a new artificial intelligence algorithm to help clinicians assess endotracheal tube placements, a necessary and important step when ventilating critically ill COVID-19 patients.
Read MoreA closer look at some of the latest airway management devices from Dale Medical, Medtronic, Hollister, Hy-Tape International, Passy Muir, and Respiralogics.
Read MoreAccording to an FDA alert, Centurion Medical Products has issued a Class I Recall for its Airway Kit containing Sheridan Endotracheal Tubes, which were previously recalled by Teleflex.
Read MoreAccording to the FDA, Teleflex Inc has issued a worldwide recall of certain lots of Hudson RCI Sheridan Endotracheal Tubes.
Read MoreA Class I recall has been issued for the Tri-Flo Subglottic Suction System from Vyaire Medical.
Read MoreTeleflex Inc is showcasing its CleanSweep Closed Suction System (CSS) at the 70th AARC Congress in Indianapolis this week. The device is an innovative closed suction catheter designed to remain in-line for up to 72 hours.
Read MoreRecent product advances in holders for the stabilization of adult and pediatric endotracheal tubes and tracheostomy tubes allow healthcare providers to minimize complications and maximize patient comfort.
Read More