Medical Device Recall Information - Philips Respironics Sleep and Respiratory Care devices, click here
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Medical Device Recall Information - Philips Respironics Sleep and Respiratory Care devices
In 2021, Philips Respironics recalled more than 15 million breathing machines produced from 2009 until 2021 because of problems involving the foam used in manufacturing. It was found that the foam deteriorates and could cause significant health issues like cancer over time. Guam residents are included in the voluntary recall of CPAP and BiPAP respirator products, according to a response by the Philips Respironics to a letter sent by Attorney General Leevin T. Camacho and attorneys general from other territories. Click here for more info.
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