Αποτελέσματα Αναζήτησης
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...
Voluntary Recall Information. Philips Respironics Sleep and Respiratory Care devices. 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).
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...
4 Φεβ 2024 · The FDA said it has received more than 116,000 reports of foam breaking down in Philips CPAP and BiPAP devices since April 2021. The company has recalled millions of the machines and agreed to pay $479 million to compensate users in a settlement.
Certain Philips Respironics DreamStation CPAP and BiPAP Machines are recalled because they may not deliver the right correct amount of breathing support.
29 Ιαν 2024 · Which sleep and respiratory care products are affected by the recall notification/field safety notice*? The affected CPAP, BiPAP sleep therapy and ventilator devices can be found at www.philips.com/src-update.
In June 2021, Philips initiated a voluntary recall notification / field safety notice for certain CPAP and BiPAP sleep therapy devices and mechanical ventilators to address potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam in these devices.
