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

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

    ResMed was recalling some models of its continuous positive airway pressure (CPAP) masks, AirFit and AirTouch, due to possible magnetic interference with certain medical devices and implants which ...

  3. 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 ...

  4. 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.

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

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

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  6. Product recall - Wikipedia

    en.wikipedia.org/wiki/Product_recall

    Product recalls are one of a number of corrective actions that can be taken for products that are deemed to be unsafe. The recall is an effort to limit ruination of the corporate image and limit liability for corporate negligence, which can cause significant legal costs. It can be difficult, if not impossible, to determine how costly can be ...

  7. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall.

  8. FDA Food Safety Modernization Act - Wikipedia

    en.wikipedia.org/wiki/FDA_Food_Safety...

    Every 2 years in even numbered years, every registered facility would be required to renew its registration between October 1 and December 31. Registration would be accepted by fax, mail and electronics means on the FDA food facility registration website. As of January 22, 2014, there were 195,518 food facilities registered with the FDA. [37]

  9. Total Recall: Target Children's Frog Mask, More Listeria ...

    www.aol.com/2011/10/21/total-recall-target...

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