Tag: Philips

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FDA Issues Safety Alert for Philips CPAP Machine

The FDA issued a safety communication to the public on reports involving thermal issues with a Philips Respironics CPAP machine.

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Reworked Philips Ventilators Get Class I Recall for Potential Foam Debris Issues

Philips Respironics recalled certain reworked ventilators for issues related to foam adhesion failure and foam debris.

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Development of Philips Detector Angio CT Solution Make Headway

Philips' Spectral Angio CT suite aims to bring the company’s spectral CT imaging technology into an integrated hybrid angio CT suite.

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FDA Issues Safety Alert for Philips CPAP Machine

The FDA issued a safety communication to the public on reports involving thermal issues with a Philips Respironics CPAP machine.

Sleep Apnea Devices Show ‘Very Low’ Amount of Degraded Foam, Philips Says

Jun 30, 2022

A recall related to one of Philips sleep apnea devices may not have been as serious or widespread as previously believed.

‘This is Not a Good Situation’: Philips Engineer Flagged Ventilator Foam Issues Years Before Recall, Court Docs Show

Jun 16, 2022

A year after Philips initiated a safety recall of its ventilators, it was discovered that the company had long been aware of certain issues.

FDA Gets Over 21,000 Medical Device Reports, Including 124 Deaths, Linked to Philips Foam Breakdown

May 24, 2022

The FDA updated a safety communication regarding medical device reports associated with the breakdown of materials used in Philips devices.

Government Warns on Cybersecurity Issues with Philips’ e-Alert MRI Monitoring System

Mar 31, 2022

Royal Philips received a cybersecurity vulnerability notice from the CISA for its e-Alert MRI system monitoring platform.

FDA Orders Philips to Notify Patients of Recall of Certain Breathing Assistance Machines

Mar 11, 2022

The FDA issued a notification order to Philips Respironics requiring the company to of the recall of certain breathing assistance machines.

Cardiac Output Monitor Interface Gets Compatibility with Philips Patient Monitoring System

Mar 3, 2022

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.

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U.S. FDA Labels Philips Expanded Ventilator Recall as Most Serious

Certain Philips ventilators that were recalled last year may lead to injuries or death, according to a new classification of the recall by the FDA.