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  2. US FDA identifies recall of ResMed's respiratory devices as ...

    www.aol.com/news/us-fda-identifies-recall-resmed...

    The FDA said ResMed was recalling these masks to update the labels and add more warnings and information. The California-based medical device maker started the recall process on Nov. 20 and has ...

  3. ResMed (RMD) Rallies as Philips Falters on Mass Product Recall

    www.aol.com/news/resmed-rmd-rallies-philips...

    The full U.S. launch of ResMed (RMD) AirSense 11 is expected any time in 2021, which might receive bigger market acceptance capitalizing on its current peer position. ResMed (RMD) Rallies as ...

  4. ResMed says its masks to remain on market despite FDA ... - AOL

    www.aol.com/news/resmed-says-masks-remain-market...

    The FDA defines a recall as a method of removing or correcting products that are in violation of laws administered by the health regulator and does not include a market withdrawal. ResMed's masks ...

  5. ResMed - Wikipedia

    en.wikipedia.org/wiki/ResMed

    ResMed Inc. is an American medical equipment company based in San Diego, California.It primarily provides cloud-connectable medical devices for the treatment of sleep apnea (such as CPAP devices and masks), chronic obstructive pulmonary disease (COPD), and other respiratory conditions.

  6. Non-invasive ventilation - Wikipedia

    en.wikipedia.org/wiki/Non-invasive_ventilation

    Non-invasive ventilation (NIV) is the use of breathing support administered through a face mask, nasal mask, or a helmet. Air, usually with added oxygen, is given through the mask under positive pressure; generally the amount of pressure is alternated depending on whether someone is breathing in or out.

  7. 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.

  8. Product recall - Wikipedia

    en.wikipedia.org/wiki/Product_recall

    A product recall is a request from a manufacturer to return a product after the discovery of safety issues or product defects that might endanger the consumer or put the maker or seller at risk of legal action. Product recalls are one of a number of corrective actions that can be taken for products that are deemed to be unsafe.

  9. Will Richland school officials face recall over a COVID mask ...

    www.aol.com/news/richland-school-officials-face...

    The recall group will need to collect about 5,000 signatures per board member to put their names to the recall ballot. Recall petitions that make it to the ballot need 50% of the vote, plus 1, to ...

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