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 ...

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 ...

The announcement adds to long-standing recall struggles with Philips sleep therapy products. For more than two years the company has been recalling some devices over health concerns related to ...

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 ...

At least two deaths and over a hundred injuries have been linked to a malfunctioning heart monitoring device from Philips and its subsidiary, Braemer. The company affirmed in a statement that that the ...

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 ...

Health risks related to the issue include longer periods of undetected or untreated irregular heartbeats and death. Philips sent customers a letter about the recall on Dec. 18, 2024, according to the ...

The FDA announced today that a Philips (NYSE: PHG) + recall involving remote cardiac monitoring software is Class I, its most serious recall designation. On Dec. 18, 2024, Philips and its ...

Starting in 2021, Philips launched a series of product recalls affecting its Respironics ... due to problems with the foam used to soundproof the devices breaking down and being inhaled by ...

Philips has issued a recall for select sleep apnea machines and ventilators over concerns that a foam component may disintegrate and be inhaled by the user possibly causing health issues including ...