FDA Announces Medtronic Surgical Device Recall Over Safety Concerns
The U.S. Food and Drug Administration (FDA) has issued a recall for several Medtronic aortic root cannula devices due to safety risks. Affected devices, used
The U.S. Food and Drug Administration (FDA) has issued a recall for several Medtronic aortic root cannula devices due to safety risks. Affected devices, used
Mid and South Essex NHS Foundation Trust (MSE FT) is leading the way in digital healthcare transformation with the rollout of the MyStaff App, an
Shockwave Medical, part of Johnson & Johnson MedTech, has enrolled the first patient in its FORWARD CAD clinical trial, marking a significant step in testing
ICU Medical has announced FDA 510(k) clearance for key additions to its IV infusion lineup, marking the launch of a new category in precision infusion
Cala Health has unveiled new clinical results supporting its TAPS therapy for treating essential tremor (ET), showcased at the American Academy of Neurology (AAN) meeting.
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