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The US Food and Drug Administration (FDA) has issued a Class I classification to Medline’s recall of endotracheal tubes following reports of device failures. Class I indicates the agency's most ...

International resuscitation guidelines recommend clinical assessment and exhaled CO 2 to confirm tube placement immediately after intubation. However, exhaled CO 2 devices can display false negative ...

Ventilator-associated pneumonia (VAP) is a major nosocomial infection that results in significant morbidity, mortality, and health care costs. Most strategies to reduce VAP attempt to decrease rates ...

Medline told customers of 89 lots of endotracheal tubes to destroy inventory after receiving reports of the inflation tube tearing and detaching, the FDA said June 11. The medical devicemaker’s Sub-G ...

Respiratory.ventilation The FDA recommends that health care providers be aware of the increased risk, and follow the instructions for use in the device labeling. Silicone-based electromyogram (EMG) ...

In a proof-of-concept study, researchers at Children's Hospital of Philadelphia (CHOP) have created a coating that can be applied to endotracheal tubes and release antimicrobial peptides that target ...

In a proof-of-concept study, researchers have created a coating that can be applied to endotracheal tubes and release antimicrobial peptides that target infectious bacteria with specificity. The ...

A Hiroshima University study of more than 31,000 patients found that pneumonia occurred more often after breathing tubes were ...

CHICAGO -- Using endotracheal tubes (ETTs) coated with ceragenins did not reduce the incidence of ventilator-associated pneumonia (VAP) compared to standard subglottic suction ETTs, but mortality was ...

WAYNE, Pa., June 21, 2023 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care and surgery, has announced a global recall of ...