May 31
Medline Industries, LP Issues Nationwide Recall of SubG Endotracheal Tube with Subglottic Suction
Medical Devices
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FDA Commissioner Dr. Robert M. Califf discusses nutrition and offers a peek at some new packaging label prototypes.
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Health professionals, consumers and patients can voluntarily report observed or suspected adverse events for human medical products to FDA. Voluntary reporting can help FDA identify unknown risk for approved medical products.
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Medical Devices
May 30
Medical Devices
May 30
Medical Devices, Radiation-Emitting Products
The agency is launching a new campaign today called “Prescribe with Confidence” to help raise awareness about OUD and to provide resources for clinicians.
As the FDA observes Clinical Trials Day, we reflect on the progress made and the widespread efforts underway to advance clinical trial innovation.
Since its inception in 1994, OWH has been at the forefront of ensuring that the unique health needs of women are met through a multifaceted approach.
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