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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Invictus Seeks to Commercialize NICU Active Noise Control Device
Invictus Medical has submitted a De Novo application to the FDA for its Neoasis incubator-based active noise control device.
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FDA Removes N95 Respirators from Medical Device Shortage List
The U.S. FDA announced the removal of N95 respirators from its medical device shortage list, signaling that demand no longer exceeds supply.
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Medtronic Recalls Ventricular Assist Device Batteries
Medtronic is recalling HeartWare Ventricular Assist Device System batteries due to their ability to experience electrical faults that cause them to unexpectedly fail.
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