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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Delving Into the Right to Repair
Moore reveals where he stands on the Right to Repair and why he believes there’s a lot of “misinformation” and “misunderstanding” surrounding the issue. He also shares his thoughts about the FDA’s “Collaborative Community” initiative and how it could’ve been more successful.
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