FDA Demands Philips Inform All Patients of Breathing Machine Recall
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. To 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. We will answer your questions at no charge.