SoClean, a Peterborough-based manufacturer of ozone-based sleep apnea machine cleaners, has filed a $200 million lawsuit against the Dutch medical equipment giant Philips, saying the company falsely ...

SILVER SPRING, Md., Feb. 27, 2020 /PRNewswire/ -- Today, the U.S. Food and Drug Administration is issuing a Safety Communication to inform patients and health care providers that devices claiming to ...

Over a year into its recall of more than 5 million respiratory devices distributed around the world, Philips this week reported the results of its testing on the polyester-based polyurethane (PE-PUR) ...

To continue reading this content, please enable JavaScript in your browser settings and refresh this page. Two Kansas City-area law firms are representing clients ...

Philips recalled millions of ventilators and sleep apnea machines in June, citing degrading foam used to dampen the machines' sound. So why is the leading manufacturer of ozone cleaners now suing ...

Electronics manufacturing giant Philips is recalling millions of CPAP and BiPAP devices due to an issue that could potentially pose a health risk to users of the machines. In the wake of the recall, ...

LiViliti Health Products has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Paptizer 360.

Almost two full years into its Class I recall of more than 5 million respiratory devices, Philips has wrapped up safety tests covering nearly all of the affected models—and is reiterating its previous ...

(Reuters) - Dutch medical equipment company Philips has been hit with a $200 million lawsuit accusing it of deceiving the public and the healthcare industry by falsely linking the problems with its ...