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 its ... products since June 2021 when it issued a recall of 15 million devices. The devices contain polyester-based polyurethane foam, which can break down and be inhaled ...

The FDA is elevating a recall from Philips related to one of its wearable outpatient heart monitors, used to help detect cases of hidden, transient arrhythmias that may only last minutes at a time.

During its first-quarter earnings report this spring, Philips, the health technology ... problems with "sound abatement foam" used in them, per the company's recall letter. The foam "may degrade ...

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 ...