FDA: Philips Respironics Must Fix or Refund Recalled Sleep Devices - Consumer Notice

Retrieved on: 2024-04-16 18:32:53

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Modes of mechanical ventilation

Food and Drug Administration

Medical equipment

Philips

Respironics

Continuous positive airway pressure

Medical device

Federal Food, Drug, and Cosmetic Act

Non-invasive ventilation

Sleep apnea

FDA Center for Devices and Radiological Health

Gerald McGinnis

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FDA: Philips Respironics Must Fix or Refund Recalled Sleep Devices - Consumer Notice. View article details on hiswai:

Excerpt

The consent decree mandates a recall remediation plan to offer all affected patients new devices, reworked machines or partial refunds, following a ...

Article found on: www.consumernotice.org

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