Medical Device Recall Notification – Philips Respironics Sleep and Respiratory Care Devices
On June 14, 2021, Philips issued a recall notification for the United States for specific affected ventilation and sleep apnea devices. The notification informs patients, users and customers of potential impacts on patient health and clinical use related to this issue. Read below to learn more about the recall, determine if your device is impacted, and next steps to register your device.
Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group
This manuscript represents a re-evaluation of keto-genic diet best practices, 10 years after the previous guideline publication.
Ten Clinical Tips on COVID-19 for Healthcare Professionals
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