US Med-Equip and Sentec Partner on Critical Respiratory Care
US Med-Equip (USME) and Sentec have partnered to provide advanced respiratory monitoring solutions for critically ill patients.
Tag: respiratory equipment
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Telesair Bonhawa High Flow Oxygen Therapy System Nabs FDA Clearance
The FDA has cleared Telesair's Bonhawa High Flow Oxygen Therapy system, which is designed to enhance treatment of patients with respiratory insufficiency.
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Viemed Acquires Home Medical Products Inc
Viemed Healthcare Inc is acquiring Home Medical Products Inc, a large regional provider of respiratory-focused home medical solutions.
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US Med-Equip and Sentec Partner on Critical Respiratory Care
US Med-Equip (USME) and Sentec have partnered to provide advanced respiratory monitoring solutions for critically ill patients.
Frustrations Grow Over Company’s Response to CPAP Recalls
Philips has experienced thousands of complaints, lawsuits, criminal investigations, and a potential DOJ settlement related to CPAP recalls.
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Medtronic to Separate its Combined Patient Monitoring & Respiratory Interventions Businesses
Medtronic intends to pursue a separation of the company’s combined patient monitoring and respiratory Interventions businesses.
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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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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.
