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FDA (Device enforcement)Recalled 2025-06-30class i

Philips Respironics, Inc.: DreamStation Auto BiPAP. Non-Continuous Ventilator.

Hazard

Devices may possess a programming error resulting in an incorrect device configuration.

Details from the source

Reason for recall: Devices may possess a programming error resulting in an incorrect device configuration. Distribution: Worldwide - US Nationwide in the states of AL, CA, CO, FL, GA, IN, LA, MD, NE, NJ, NY, PA, TX & DC. The country of France. Quantity: 8 units Lot/code info: Model No. UDSX700S11F; UDI: 606959429772; Serial No. J18909076CC90, J2091514323C5, J2164570462CB, J23391208BCBE, J26552747A030, J2909781691D2, J294724447698, J301490021E77.

UPC codes

606959429772

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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