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Product Recalls & Refunds Online / National

Philips Respironics, Inc.: DreamStation Auto CPAP. Non-Continuous Ventilator.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Devices may possess a programming error resulting in an incorrect device configuration.. Recalled by Philips Respironics, Inc.. 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.. Classification (Class I — serious health hazard). Affected lots/dates: Model No. UDSX500S11F; UDI: 606959429765; Serial No. J204432084D03, J206957368810, J207023218478, J21450857096A, J219786. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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