Vyaire Medical Recalls AirLife Manual Resuscitators
The Class I recall of certain AirLife manual resuscitators is due to a manufacturing defect that may prevent patients from receiving enough ventilation, which could lead to injury or death.
The Class I recall of certain AirLife manual resuscitators is due to a manufacturing defect that may prevent patients from receiving enough ventilation, which could lead to injury or death.
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.
Gerald E. McGinnis, founder of Respironics and creator of the first CPAP machine to treat sleep apnea, died on Jan 25 at age 89.
The FDA granted 510(k) clearance to Masimo’s Stork, a baby monitoring system, for prescription use with healthy and sick babies 0-18 months of age.
The FDA has alerted healthcare providers about potential exposure to elevated levels of formaldehyde when GE Healthcare accessory compressors are used with certain ventilators.
Studies show that those with long COVID may benefit from physical therapy services as soon as they are able to tolerate physical activity.