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  2. Urgent Medical Device Recall Issued for Ventilator - AOL

    www.aol.com/urgent-medical-device-recall-issued...

    Baxter International Inc. recalled the ventilators because of reports that they aren’t charging properly.

  3. These machines to help people breathe were recalled a year ...

    www.aol.com/news/machines-help-people-breathe...

    Safety concerns led Philips Respironics to recall millions of respiratory machines. A year later, many are still using them despite the possible risks. These machines to help people breathe were ...

  4. List of ventilator manufacturers - Wikipedia

    en.wikipedia.org/wiki/List_of_ventilator...

    Mobile ventilators [2] Manufacturer Country Market share (2019) Dräger: Germany 24 % Weinmann Medical: Germany 21 % Hamilton Medical: U.S., Switzerland 18 % Vyaire Medical: U.S. 5 % Customs Japan 4 % O Two Canada 4 % Smiths Medical U.S. 4 % Medtronic: Ireland, U.S. 4 % Air Liquide Healthcare France 3 % (and 13 other vendors contributing for 13%)

  5. Philips cites health risks in recall of ventilators and sleep ...

    www.aol.com/philips-cites-health-risks-recall...

    The medical technology and equipment giant Philips has recalled some of its ventilators and CPAP machines due to a form piece that could potentially become toxic and cause cancer in its users.

  6. Respironics - Wikipedia

    en.wikipedia.org/wiki/Respironics

    Philips Respironics's products include devices for the diagnosis and treatment of sleep apnea including CPAP and bi-level non-invasive ventilation machines, oxygen concentrators for patients requiring supplemental oxygen, infant apnea monitors for infants at risk of SIDS, asthma treatment solutions and hospital ventilators.

  7. Continuous positive airway pressure - Wikipedia

    en.wikipedia.org/wiki/Continuous_positive_airway...

    Both modalities stent open the alveoli in the lungs and thus recruit more of the lung surface area for ventilation. However, while PEEP refers to devices that impose positive pressure only at the end of the exhalation , CPAP devices apply continuous positive airway pressure throughout the breathing cycle.

  8. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.

  9. Philips issues voluntary recall for CPAP machines, ventilators

    www.aol.com/news/philips-issues-voluntary-recall...

    Jun. 15—Medical equipment company Philips has issued a recall on some products to address possible health risks associated with a foam component meant to help reduce noise. The polyester-based ...