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Updates on Philips Respironics CPAP, BiPAP, and Ventilator Recall
Today, the U.S. Food and Drug Administration (FDA) updated the frequently asked questions (FAQs) about this recall on FDA.gov: Philips Respironics CPAP, BiPAP, and Ventilator Recall: Frequently Asked Questions. The updates include answers to questions such as:
- When will the devices start to be repaired or replaced?
- What is the status of Philips Respironics’ plans for repairing or replacing the devices?
- What is the FDA’s role in the Philips Respironics recall?
- I use one of the affected devices daily. I can’t wait for a new device. What can I do now?
The FDA is committed to using every tool at our disposal to increase the availability of these medical products. The FDA is working with Philips Respironics to monitor the repair or replacement of impacted devices as expeditiously as possible and is continuing to gather information to inform our actions. We are collaborating with other manufacturers and government partners to support availability of CPAP and BiPAP machines.
Questions?
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.
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