FDA Announces Recall of Certain Sleep and Respiratory Devices
Friday, July 23, 2021
Reprinted with permission from the Defense Health Agency, Communications Division
The Food and Drug Administration (FDA) has directed Philips Respironics to recall millions of sleep and respiratory devices following concerns that foam in the devices, which is used to reduce sound and vibration, may break into particles and enter the air hose of the device and be inhaled by the user. In response, the Military Health System (MHS) has notified all TRICARE-authorized durable medical equipment providers of the recall. And it’s asking prescribing physicians to help notify patients of the recall and determine if they were issued a medical device on the Philips recall list.
Read more at tricare.mil.