And The Hits Just Keep On Coming: Another Class I Recall For Philips Breathing Devices

The US FDA has designated another recall of Philips breathing devices as class I, its most serious type. The recall includes about a thousand devices that had previously been reworked during a June 2021 initial recall.

Philips Respironics initiated a recall in February of more DreamStation devices, this time including various reworked CPAP and BiPAP models. The latest recall covers 1,088 machines distributed in the US between 1 December 2021 and 31 October 2022.

In its recall notice published 7 April, the Food and Drug Administration noted that these devices were part of...