Philips Files Lawsuit Against PSN Labs Over Foam Recall Damage
Philips has filed a lawsuit against PSN Labs, claiming incorrect analysis of foam material used in recalled ventilation devices.
Philips has filed a lawsuit against PSN Labs, claiming incorrect analysis of foam material used in recalled ventilation devices.
The FDA has issued a safety alert regarding Philips Respironics' DreamStation 2 CPAP machines due to reports of safety issues, including fire, smoke, burns, and overheating, and is working with the company to address the problem and provide safety recommendations to users.
Philips Respironics recalled certain reworked ventilators for issues related to foam adhesion failure and foam debris.
Philips has filed a lawsuit against PSN Labs, claiming incorrect analysis of foam material used in recalled ventilation devices.
Philips’ Spectral Angio CT suite aims to bring the company’s spectral CT imaging technology into an integrated hybrid angio CT suite.
Read MorePhilips has recalled certain masks used with bilevel positive airway pressure machines and CPAP machines due to a serious safety concern.
Read MorePhilips RS North America a manufacturer of durable medical equipment agreed to pay over $24 million to resolve False Claims Act allegations.
Read MorePhilips recalled certain bi-level positive airway pressure machines that may contain a plastic contaminated with a non-compatible material.
Read MoreThe FDA updated a safety communication regarding the ongoing recall issues of Philips’ respiratory devices.
Read MoreRoy Jakobs is tapped to succeed Frans van Houten as Royal Philips’ president and CEO, effective October 15. Jakobs has been critical in helping Philips address ongoing medical device recall challenges, the company says.
Read MorePhilips may be looking to bring an end to its ongoing plight of medical device recalls via a settlement agreement with the DOJ.