In June 2021, Philips Respironics issued a recall on some of their BiLevel CPAP and PAP machines, including their mechanical ventilators that were sold to consumers in the United States. They issued a similar warning to their international customers. The reason for the recall is due to a compo...
Philips/Respironics recently announced a recall on some of their medical devices including CPAP machines. For more information, or to check if your device is affected by this recall, click the link below: https://www.usa.philips.com/healthcare/e/sleep/communications/src-update...
The recall involves specific Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP) and mechanical ventilator devices to address potential health risks related to polyester-based polyurethane sound abatement foam that is in the machines, Philips said in a...
Please be sure to enter the serial number from your CPAP, BiLevel PAP or ventilator device directly and not the number from an attached humidifier or water tank. You can find help on how to locate your serial numberhereor call877-907-7508 ...
Philips has racked up its sixth recall related to its continuous positive airway pressure (CPAP) device from the U.S. Food and Drug Administration (FDA) on Oct. 19. The company first began a recall of around 5.5 million devices used by sleep apnea patien
The FDA also notified users that this recall notice is not associated with the foam issue impacting certain BiPAP machines, which had been recalled in June 2021, but it "does apply to some of the devices." CERTAIN PHILIPS RESPIRONICS VENTILATORS, CONTINUOUS POSITIVE AIRWAY PRESSURE (CPAP) AND ...
The recall was issued to address the breaking down of the polyester-based polyurethane (PE-PUR) foam used in these devices to reduce sound and vibration.
Philips Recalls CPAP Machines On June 30, 2021, the U.S. Food and Drug Administration issued aSafety Communicationabout Philips’ voluntary recall of some of its BiPAP, CPAP and ventilator devices. Philips is the largest producer of CPAPs in the world, as many as four million machines could...
Philips Respironics, a manufacturer of CPAP devices, and the FDA issued a recall for their machines in June 2021, after it was discovered that users were likely to inhale or ingest toxic gasses and particles from a part of the machine designed to limit sound and vibration. Among the possible...
Philips Respironics CPAP/BiPAP Recall Notice and Up-to-Date FAQ (Updated regularly). Register Your CPAP Units For Free Service.