[{"@context":"https:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/www.wardblacklaw.com\/blog\/fda-demands-philips-inform-all-patients-of-breathing-machine-recall\/#BlogPosting","mainEntityOfPage":"https:\/\/www.wardblacklaw.com\/blog\/fda-demands-philips-inform-all-patients-of-breathing-machine-recall\/","headline":"FDA Demands Philips Inform All Patients of Breathing Machine Recall","name":"FDA Demands Philips Inform All Patients of Breathing Machine Recall","description":"The FDA has recently issued an order requiring Philips Respironics to inform all patients that there has been a recall of some of their breathing machines. \u00a0To learn more about the recall and the new FDA orders, follow the link below. If you or someone you know has used a recalled CPAP machine by Philips […]","datePublished":"2022-03-11","dateModified":"2022-10-10","author":{"@type":"Person","@id":"https:\/\/www.wardblacklaw.com\/blog\/author\/kelseyhecker\/#Person","name":"Kelsey Hecker","url":"https:\/\/www.wardblacklaw.com\/blog\/author\/kelseyhecker\/","identifier":15,"image":{"@type":"ImageObject","@id":"https:\/\/secure.gravatar.com\/avatar\/c63807b0daa86af6e09e3f462917c191cf025d381f5a57b5df336f2964d26727?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/c63807b0daa86af6e09e3f462917c191cf025d381f5a57b5df336f2964d26727?s=96&d=mm&r=g","height":96,"width":96}},"publisher":{"@type":"Organization","name":"Ward Black Law","logo":{"@type":"ImageObject","@id":"https:\/\/www.wardblacklaw.com\/wp-content\/uploads\/2022\/04\/logo.png","url":"https:\/\/www.wardblacklaw.com\/wp-content\/uploads\/2022\/04\/logo.png","width":116,"height":119}},"image":{"@type":"ImageObject","@id":"https:\/\/www.wardblacklaw.com\/wp-content\/uploads\/2022\/03\/fda-demands-philips-inform-all-patients-of-breathing-machine-recall.jpg","url":"https:\/\/www.wardblacklaw.com\/wp-content\/uploads\/2022\/03\/fda-demands-philips-inform-all-patients-of-breathing-machine-recall.jpg","height":334,"width":500},"url":"https:\/\/www.wardblacklaw.com\/blog\/fda-demands-philips-inform-all-patients-of-breathing-machine-recall\/","about":["News"],"wordCount":98,"articleBody":"The FDA has recently issued an order requiring Philips Respironics to inform all patients that there has been a recall of some of their breathing machines. \u00a0To learn more about the recall and the new FDA orders, follow the link below.If you or someone you know has used a recalled CPAP machine by Philips and is experiencing medical complications such as cancer or breathing issues among others, call or text our office at (336) 333-2244. \u00a0We will answer your questions at no charge.FDA Orders Philips Respironics to Notify Patients Regarding the Recall of Certain Breathing Assistance Machines"},{"@context":"https:\/\/schema.org\/","@type":"BreadcrumbList","itemListElement":[{"@type":"ListItem","position":1,"name":"Blog","item":"https:\/\/www.wardblacklaw.com\/blog\/#breadcrumbitem"},{"@type":"ListItem","position":2,"name":"FDA Demands Philips Inform All Patients of Breathing Machine Recall","item":"https:\/\/www.wardblacklaw.com\/blog\/fda-demands-philips-inform-all-patients-of-breathing-machine-recall\/#breadcrumbitem"}]}]