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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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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French Prosecutors Launch Criminal Investigation Into Philips Ventilator Recall
Philips’ ventilator recall woes, which stemmed from the machines causing patient health issues, are under investigation by French prosecutors.
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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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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.
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