Class I

Medical Device Recall: DreamStation Auto CPAP. Non-Continuous Ventilator.

Philips Respironics, Inc. · June 30, 2025

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.

States Affected

NATIONWIDE

Quantity Affected

57 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2227-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.