Medical Device Recall Information - Philips Respironics Sleep and ...
In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside …
Recalled Philips Ventilators, BiPAP Machines, and CPAP Machines
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...
Philips BiPAP machine recall associated with 8 deaths
Aug 5, 2025 · Philips recalled three models of BiPAP machines last year due to an alarm that can cause the machines to shut down. The Food and Drug Administration posted a notice on Monday, noting …
Philips CPAP Recall: Updates & FDA Safety News - Drugwatch
Mar 7, 2025 · Philips Respironics recalled and then replaced specific CPAP, BiPAP and ventilator machines in 2021 and 2022 because of health risks from the breakdown of PE-PUR foam. The FDA …
FDA Updates Injury, Death Reports from Ventilator Inoperative Alarm ...
Aug 5, 2025 · This week, the Food and Drug Administration (FDA) issued an update to its 2024 recall notice of Philips BiPAP V30, A30, and A40 ventilators related to the risk for a failure in the ventilator …
FDA updates on serious Philips CPAP, BiPAP device recall
Sep 15, 2025 · Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death. It marks the latest recall development for the...
Contact and support for Philips Respironics voluntary recall
Registration for affected CPAP and BiPAP devices in the US and Canada closed on December 31, 2024. Contact and support options for patients impacted by the June 2021 voluntary recall of certain …
Ventilator Correction: Philips Respironics Updates Use Instructions
Aug 6, 2025 · BiPAP A30, A40, and V30 devices may shut down due to a Ventilator Interruptions, leading to therapy loss. May cause serious injury or death.
Frequently Asked Questions on Philips Recall of PAP Devices - AARC
On June 14, 2021, Philips initiated a voluntary U.S. recall (and an international field safety notice) for specific Philips Respironics models of continuous positive airway pressure (CPAP), bilevel positive …
Philips CPAP and BiLevel PAP Recall - VHA National Center for Patient ...
Philips Respironics announced a voluntary recall for certain CPAP, BiLevel PAP, and mechanical Ventilator Devices due to issues related to deterioration of the sound abatement foam used in these …