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Philips CPAP Recall Registration

  • For patients using BiLevel PAP and CPAP devices: Discontinue use of affected units and consult with physicians to determine the benefits of continuing therapy and potential risks.
  • For patients using life-sustaining mechanical ventilator devices: DO NOT discontinue or alter prescribed therapy without consulting physicians to determine appropriate next steps.
  • Only Philips or Philips Respironics machines are being recalled. Do not register another brand CPAPs.
  • Only register CPAP machine serial numbers. Do not register humidifiers (they are not in the recall list).

Philips is recommending that customers and patients halt use of ozone-related cleaning products and adhere to their device instructions for Use for approved cleaning methods.
Additionally, Philips is reminding customers and patients to review the age of their BiLevel PAP and CPAP devices, as they are typically recommended to be replaced after five years of use.

Respshop, a Philips official distributor, is authorized to collect information for Philips CPAP, Auto CPAP, and BiPAP recall. Information submitted will be sent to Philips or its authorized company for recall purposes.
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