4 results

• Philips BiPAP Recall Issued Due to Risk of Interruptions, Loss of Therapy

  June 28, 2024

  Irvin Jackson

  The FDA has determined that instructions issued by the manufacturer to fix problems linked to 65 patient deaths should be classified as a Class I recall, due to the risk of device failure which could result in loss of therapy.

• FDA Indicates Recalled Philips BiPAP Machines Pose Risk of Serious and Life-Threatening Injury

  September 28, 2022

  Russell Maas

  A Philips BiPAP machine recall has been given a class I designation by the FDA, indicating volatile organic compounds emitted from the devices could cause serious injury or death.

• Philips CPAP Masks Recalled Due to Risk Magnets May Interfere with Implants, Causing Serious Injury or Death

  September 7, 2022

  Russell Maas

  More than 17 million Philips CPAP masks are being recalled due to the risk of magnets interfering with medical implants.

• Philips BiPAP Recall Issued Over Risk Plastic in Motor May Release Toxic Chemicals

  August 30, 2022

  Russell Maas