Philips Updates Users About Aerosol Risk for Ventilators
Philips has updated instructions for several ventilators to address aerosol deposits on internal sensors when used with in-line nebulizers.
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Philips Recalls BrightView Imaging Systems
Philips has recalled its BrightView SPECT imaging systems for a potential component failure that would cause parts to fall on the patient.
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Avante Health Solutions Announces Major Right to Repair Development
Avante Health Solutions announced a significant turning point in the right to repair, specifically concerning the right to access, service, and maintain diagnostic imaging medical equipment manufactured by Philips Medical Systems for Avante's customers who own the equipment.
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Philips Updates Users About Aerosol Risk for Ventilators
Philips has updated instructions for several ventilators to address aerosol deposits on internal sensors when used with in-line nebulizers.
FDA OKs Philips Compact Ultrasound System
Philips has received 510(k) clearance from the U.S. FDA for its newest ultrasound system, the 5000 Compact Series.
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FDA Hands Philips its 5th Class I Recall of the Year for Faulty Ventilators
Philips’ recent recall regarding certain BiPAP machines has been classified as a Class I recall, according to the U.S. FDA.
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Philips RS to Pay $1.2M to Resolve Allegations of Unlawful Kickbacks
Philips RS has agreed to pay nearly $1.3 million to settle allegations that it violated the False Claims Act and Anti-Kickback Statute.
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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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Philips Respironics BiPAP and CPAP Masks Hit by Recall
Philips has recalled certain masks used with bilevel positive airway pressure machines and CPAP machines due to a serious safety concern.
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Philips Subsidiary to Pay Over $24M for Alleged False Claims for Respiratory Equipment
Philips RS North America a manufacturer of durable medical equipment agreed to pay over $24 million to resolve False Claims Act allegations.
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Certain Philips Respironics BiPAP Machines Recalled Due to a Plastic Issue, FDA Says
Philips recalled certain bi-level positive airway pressure machines that may contain a plastic contaminated with a non-compatible material.
