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Philips Respironics Device Recall
Philips Respironics announced a voluntary recall for certain CPAP, BiLevel PAP and Ventilator Devices manufactured prior to April 21, 2021.
This recall is due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices.
Philips is notifying customers and users of affected devices that they will replace the current sound abatement foam with a new material that is not affected by this issue. Affected devices currently will be either replaced with a new or refurbished unit that incorporates the new material, or repaired to replace the sound abatement foam in customer units.
For more information on the Recall Notice, a complete list of impacted products, and more information, visit philips.com/src-update .
Rotech is committed to providing safe CPAP/BiPAP and Ventilator equipment for all patients.
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