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PHILIPS® CPAP VENTILATOR AND MACHINES RECALLED

PHILIPS® CPAP VENTILATOR AND MACHINES RECALLED

Injuries linked to recalled devices may include

  • CANCERS
  • RESPIRATORY FAILURE
  • CHEMICAL POISONING
  • PLEURAL EFFUSION
  • KIDNEY/LIVER DAMAGE & DISEASE
  • CARDIOVASCULAR EVENTS
  • AND MORE..

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National US Recall Of Philips® CPAP & BIPAP Devices

June 30 2021 - Certain Phillips® Brand CPAP & BIPAP Devices Recalled Due to Potential Health Risks

The FDA is alerting consumers of the device recall due to health risks. The health risks are liked to the foam material failing resulting in possible debris and/or chemcials possibly entering the airway. These chemicals may be linked to respiratory failure, cancers and cardiovascular events and more.

Those that used certain Philips® CPAP, BIPAP Devices & ventilation machines may be eligible for substantial compensation. Free case review is available, is 100% free and comes with no obligation.

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CPAP And Ventilation Device Recall News Updates

2021

as awareness of the recall spreads, thousands of impacted patients begin to come forward and file individual claims for compensation.

2021

The CEO of Philips comes forward and states that 3 to 4 million devices will be recalled due to degrading foam.

2020

thousands of patients that use philips® cpap and ventilation devices begin to notice adverse side effects.

Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with Philips® or any government agency.

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