DreamStation Auto BiPAP. Non-Continuous Ventilator.
- Company
- Philips Respironics, Inc.
- Recall Initiated
- June 30, 2025
- Posted
- August 8, 2025
- Recall Number
- Z-2228-2025
- Quantity
- 8 units
- Firm Location
- Murrysville, PA
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.
Lot / Code Info
Model No. UDSX700S11F; UDI: 606959429772; Serial No. J18909076CC90, J2091514323C5, J2164570462CB, J23391208BCBE, J26552747A030, J2909781691D2, J294724447698, J301490021E77.
Root Cause
Process control
Action Taken
Consignees were contacted by phone from 6/30/25 to 7/02/25 to facilitate provision of a replacement device. Additionally, a "Medical Device Recall Field Safety Notice" dated 6/6/2025 was sent to consignees instructing them to continue using their affected device until Philips Respironics can ship them a replacement. DMEs are to share the notice with those who need to be aware within their organization and to organizations where devices were transferred. If a consignee received the written notice but not a phone call from Philips Respironics, they are to call 1-877-387-3311 or email PatientSupport@philips.com. Consignees with any questions can contact Philips Respironics at 1-800-345-6443 (prompts 4, 5).