FDA MedWatch - Update on Philips Respironics Ventilators, BiPAP Machines, and CPAP Machines June 2021 Recall

The FDA is providing the latest information about medical device reports associated with the PE-PUR foam breakdown in recalled devices

If your email program has trouble displaying this email, view as a webpage. MedWatch - The FDA Safety Information and Adverse Event Reporting Program Update on Philips Respironics Ventilators, BiPAP Machines, and CPAP Machines June 2021 Recall Today, the U.S. Food and Drug Administration (FDA) is providing the latest information about medical device reports (MDRs) received from May 1 to July 31, 2022, that are associated with the breakdown of the polyester-based polyurethane (PE-PUR) foam used in the Philips Respironics ventilators, BiPAP machines, and CPAP machines included in the June 2021 recall. The FDA will continue to update the public about the status of the Philips Respironics June 2021 recall. Read More Sign up to receive email alerts Subscribe to Philips CPAP, BiPAP, and Ventilator Recall email list for new or updated content that is specifically related to the Philips CPAP, BiPAP, and Ventilator Recall. Questions? The FDA.gov website includes FAQs on Philips Respironics Ventilator, BiPAP Machine, and CPAP Machine Recalls to address questions about the recalls and provide additional resources with more information.   For more information on the recall notification, contact your local Philips representative or visit Philips Respironics' recall notification page. More information on medical device recalls, including What is a Medical Device Recall, is available on FDA.gov. Follow us on Twitter at @FDAMedWatch

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