PlainRecalls
FDA Devices Critical Class I Ongoing

DreamStation Auto. Non-Continuous Ventilator.

Reported: August 20, 2025 Initiated: June 30, 2025 #Z-2229-2025

Product Description

DreamStation Auto. Non-Continuous Ventilator.

Reason for Recall

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

Details

Recalling Firm
Philips Respironics, Inc.
Units Affected
28 units
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.
Location
Murrysville, PA

Frequently Asked Questions

What product was recalled?
DreamStation Auto. Non-Continuous Ventilator.. Recalled by Philips Respironics, Inc.. Units affected: 28 units.
Why was this product recalled?
Devices may possess a programming error resulting in an incorrect device configuration.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 20, 2025. Severity: Critical. Recall number: Z-2229-2025.