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  2. Philips (PHG) Recalls CPAP, Ventilators Used for Sleep Apnea

    www.aol.com/news/philips-phg-recalls-cpap...

    Philips (PHG) is recalling some Bi-Level PAP, CPAP, and mechanical ventilator devices in the United States due to health risks. Philips (PHG) Recalls CPAP, Ventilators Used for Sleep Apnea Skip to ...

  3. A $1 billion CPAP recall devastated Philips. The CEO ... - AOL

    www.aol.com/finance/1-billion-cpap-recall...

    A $1 billion CPAP recall devastated Philips. The CEO’s turnaround plan involves overhauling company culture and adding a key role to the C-suite. Phil Wahba. Updated October 4, 2024 at 9:29 AM.

  4. Respironics - Wikipedia

    en.wikipedia.org/wiki/Respironics

    During the pandemic, Philips conducted a series of studies on the foam, showing the deteriorating foam and chemicals released by it, which could cause "serious injury, life-threatening or permanent impairment". [2] The company said patients' health is its top priority, and regretted the "distress and concern" that the recall caused.

  5. 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 ...

  6. 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.

  7. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    FDA guidelines for companies to follow when recalling defective products under the Agency's jurisdiction are published in Title 21 of the Code of Federal Regulations, Part 7. These guidelines make clear that FDA expects these firms to take full responsibility for product recalls, including follow-up checks to assure that recalls are successful.

  8. Recall of Philips Manufacturer's Sleep Apnea Device - AOL

    www.aol.com/recall-philips-manufacturers-sleep...

    Philips said potentially harmful disintegrating foam that could be inhaled is the culprit. Simmons is a neurologist who treats sleeping disorders. Recall of Philips Manufacturer's Sleep Apnea Device

  9. List of Mullard–Philips vacuum tubes - Wikipedia

    en.wikipedia.org/wiki/List_of_Mullard–Philips...

    Most post-war European thermionic valve (vacuum tube) manufacturers have used the Mullard–Philips tube designation naming scheme. Special quality variants may have the letter "S" appended, or the device description letters may be swapped with the numerals (e.g. an E82CC is a special quality version of an ECC82)