This is not the only recall the company is dealing with. Philips’ Respironics business has been facing issues with some of its sleep apnea products since June 2021 when it issued a recall of 15 ...

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 ...

Multinational electronics and medical device manufacturer Philips has made headlines lately for all the wrong reasons. The recent recall of its SPECT BrightView nuclear imaging system is the ...

USA TODAY has reached out to the attorneys for comment. Philips announced a recall for millions of their Bi-Level Positive ...

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.

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 ...

Starting in 2021, Philips launched a series of product recalls affecting its Respironics range of ventilators and other respiratory machines; most recently, a Class I recall of around 63,000 ...

to immediately cease the sale of certain products manufactured by affiliates of Philips Lighting brand, and also ordered the recall and destruction of infringing products distributed in the market ...

The Court ordered Conrad Electronic, the global distributor where these products are sold, to immediately cease the sale of certain products manufactured by affiliates of Philips Lighting brand, and ...