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Philips Respironics, Inc.: Philips DreamStation Auto BiPAP and CPAP, Model

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

Recall reason: A limited number of remediated Philips DreamStation units may experience communication issues when connecting to the cloud-based care management application. Should this be the case, this may affect the ability to download prescription settings to the device or the device may have incorrect prescription settings for the patient.. Recalled by Philips Respironics, Inc.. Distribution: US Nationwide. France, Reunion.. Classification (Class I — serious health hazard). Affected lots/dates: GTIN/HIBC: HIBCUCDSX500S11, GTINUDSX500S11F, HIBCUDSX700S11, GTINUDSX700S11F, GTINUFRX500S14; Serial Numbers: J2442119. Contact the manufacturer or the retailer where you purchased this device

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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