Rather than issuing a recall, medical device managers rely on their physician-customers to screen out defective products and not use them on patients, a new behavioral study published in the Journal ...

Medical device firm managers trust physicians to screen out defects in lieu of recalls, a study conducted by Indianapolis-based Indiana University and Minneapolis-based University of Minnesota ...

The Food and Drug Administration on Wednesday sent a warning letter to St. Jude Medical, saying the devicemaker downplayed issues with its defibrillator batteries and failed to recall the devices for ...

Numerous medical devices sold in the United States are subject to active recalls. If you have a medical device that is subject to an active recall, it will be important to make sure you know what this ...

Two million bone transplants are performed worldwide yearly, including half a million in the United States alone. Yet, a QUT-led study has found surgeons are slow to adopt newly developed biomaterials ...

As part of our Spotlight series, Dennis C. Gucciardo, who counsels medical device manufacturers throughout the product lifecycle in the US Food and Drug Administration (FDA) regulatory context, shares ...

Bone defects are a major challenge in regenerative medicine, often requiring advanced biomaterials to enhance the natural healing process. Traditional bone repair methods, including bone grafts, face ...