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 ...

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 ...

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 ...

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.

When not required in the scanner room, the Dameca MRI 508 can function as a conventional anesthesia machine in the operating theatre. High-level safety features The Dameca MRI 508 has a number of ...

How long does Philips take to deliver? Philips offers shipping in 2-5 business days across the US. If you order multiple products they may be shipped separately and arrive at different times.

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 ...

Other pharmaceutical and tech news is on the FDA's drug approval system and a rapid diagnostic test for bloodstream infections. Modern Healthcare: Philips Recalls Remote Cardiac Monitoring Software ...

Forget about time-consuming, multiple tubing connections between the anesthesia machine, breathing system and patient. Our integrated breathing system (IBS) integrates an ascending bag-in-bottle ...