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Philips Respironics, Inc. recalls DreamStation Auto. Non-Continuous Ventilator.
Recalled August 20, 2025 · FDA recall Z-2229-2025 · Philips Respironics
Hazard
Devices may possess a programming error resulting in an incorrect device configuration. · FDA Class I
Units
28 units
Sold at
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.
Description
Devices may possess a programming error resulting in an incorrect device configuration.
Product
DreamStation Auto. Non-Continuous Ventilator.
Manufacturer(s)
Philips Respironics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →