Αποτελέσματα Αναζήτησης
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 U.S.) / voluntary recall notification (U.S. only).
- Information for Patients
Only devices affected by the recall/ field safety notice...
- News & Updates
News & Updates - Medical Device Recall Information - Philips...
- Ozone Cleaner Information
For detailed information about caring for your replacement...
- Contact and Support
Contact and support options for patients impacted by the...
- Information for Clinicians
Information for Clinicians - Medical Device Recall...
- Understanding The Recall Process
We understand that waiting for news about when and how your...
- Information for Business Customers
Information for Business Customers - Medical Device Recall...
- Information for Patients
5 Οκτ 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...
4 Οκτ 2024 · 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...
As a result of extensive ongoing analysis, on June 14, 2021, the company issued a recall notification for specific affected Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (BiLevel PAP) devices, and Mechanical Ventilators.
The U.S. Food and Drug Administration (FDA) is updating the June 2021 safety communication about the Philips Respironics (Philips) recalled ventilators, bilevel positive airway pressure (also...
On June 14, 2021, Philips initiated a voluntary recall/field safety notification for certain continuous positive airway pressure (CPAP), bilevel positive airway pressure (BiPAP) and mechanical ventilator devices to address potential health risks related to the polyester-based polyurethane (PE-PUR) foam in these devices, specifically the ...
29 Ιαν 2024 · Airway Pressure (PAP) device use and cancer risk: Based on 13 epidemiological studies identified from a systematic literature review, no association has been established between use of PAP devices, including Philips Respironics PAP devices, and risk of cancer in patients with obstructive sleep apnea (OSA).
