The product being recalled is Philips Respironics DreamStation1 (Uno Remediated Devices), models REP DreamStation Auto CPAP Recert, DreamStation Auto, FR REP DreamStation Auto BiPAP, DOM-RECRT, and REP DreamStation Auto CPAP, DOM – RECRT. 1,088 of these devices...
The product models affected are: REP DreamStation Auto CPAP Recert, DreamStation Auto, FR REP DreamStation Auto BiPAP, DOM-RECRT, and REP DreamStation Auto CPAP, DOM - RECRT For serial numbers, go to theMedical Device Recall Database There are 1,088 devices recalled in the U.S...