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RESPIRONICS CPAP, BiPAP, AND TRILOGY RECALL

Home Sleep and Respiratory Care Update | Philips

CLICK THE LINK ABOVE TO REGISTER YOUR DEVICE.

PLEASE CONTACT RESPIRONICS DIRECTLY AT 877-907-7508.

Phillips Respironics announced a voluntary recall on June 14, 2021 for certain CPAP, BiLevel PAP, and Trilogy devices manufactured prior to April 21, 2021.

Philips is notifying customers and users of affected devices that they will replace the current sound decreasing foam with a new material that is not affected by the 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 decreasing foam in customer units. 

FDA Safety Communication Article Released June 30, 2021

Certain Philips Respironics Ventilators, BiPAP, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication | FDA

 

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