Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

DreamStation Auto. Non-Continuous Ventilator. Recalled by Philips Respironics, Inc. Due to Devices may possess a programming error resulting in...

Date: June 30, 2025
Company: Philips Respironics, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Philips Respironics, Inc. directly.

Affected Products

DreamStation Auto. Non-Continuous Ventilator.

Quantity: 28 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Philips Respironics, Inc.

Philips Respironics, Inc. has 85 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report