The FDA issued a safety communication to the public on reports involving thermal issues with a Philips Respironics CPAP machine.
A recall related to one of Philips sleep apnea devices may not have been as serious or widespread as previously believed.Read More
‘This is Not a Good Situation’: Philips Engineer Flagged Ventilator Foam Issues Years Before Recall, Court Docs Show
A year after Philips initiated a safety recall of its ventilators, it was discovered that the company had long been aware of certain issues.Read More
The FDA updated a safety communication regarding medical device reports associated with the breakdown of materials used in Philips devices.Read More
Royal Philips received a cybersecurity vulnerability notice from the CISA for its e-Alert MRI system monitoring platform.Read More
The FDA issued a notification order to Philips Respironics requiring the company to of the recall of certain breathing assistance machines.Read More
Retia Medical has received a declaration of compatibility from Philips for its Argos cardiac output monitor to interface with Philips’ IntelliBridge system on the IntelliVue patient monitoring systems.Read More