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      • Philips Respironics Recalls Certain Continuous and Non-Continuous Ventilators, including CPAP and BiPAP, Due to Risk of Exposure to Debris and Chemicals The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
      www.fda.gov › medical-devices › medical-device-recalls
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  2. Oct 5, 2023 · In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and continuous positive airway...

  3. Apr 11, 2024 · The following Philips Respironics CPAP machines, BiPAP machines, and ventilators with manufacture dates prior to April 26, 2021 have been recalled and are not available for sale: A-Series BiPAP A30; A-Series BiPAP A40; A-Series BiPAP Hybrid A30; A-Series BiPAP V30 Auto; C-Series ASV; C-Series S/T and AVAPS; DreamStation 1; DreamStation ASV ...

  4. Sep 28, 2023 · Millions of people in the United States and around the world were affected by the June 2021 recall of Philips Respironics ventilators and CPAP and BiPAP machines. ProPublica and the...

  5. Aug 17, 2021 · The Philips recall involved certain BiPAP (bi-level positive air pressure), CPAP (continuous positive air pressure) and ventilator machines manufactured before April 26. The company has to...

  6. Oct 5, 2023 · In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and continuous positive airway...

  7. Feb 2, 2024 · Philips has agreed to stop selling sleep apnea machines in the U.S. and existing devices manufactured between 2009 and April 2021 are subject to recall, as they may pose a serious injury risk...

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