Nicko displays the device, a Philips DreamStation, to the camera, noting that it has “now been recalled.” He claims this is because the sound-abating foam inside breaks down, “and then it travels into ...

Philips announced a recall for millions of their Bi-Level Positive ... The recall was attributed to a potential defect in the devices in which foam used in them could degrade and cause inhalation ...

Philips is recalling the software associated with its mobile cardiac outpatient telemetry devices after 109 patient injuries and two patient deaths, a Jan. 13 FDA recall notice said. The software ...

Unlike conventional single event cases, mediation in mass tort cases can be more effective if the effort is applied ...

The Class I recall, the FDA’s severest classification, is a correction and does not require removing devices from where they are used or sold. Philips started the recall on Nov. 20, 2024 ...