FDA Warns Doctors of Abbott Trifecta Valve Deterioration Risks
The FDA warns that Abbott Trifecta heart valve implants may deteriorate within only a few years, leading to the need for valve replacement and increasing the risk of patient death.
The FDA warns that Abbott Trifecta heart valve implants may deteriorate within only a few years, leading to the need for valve replacement and increasing the risk of patient death.
A letter by Senator Elizabeth Warren accuses Abbott Laboratories of hiding previous infant formula cronobacter problems through aggressive legal tactics.
The FDA warns that MitraClip heart valve repair devices may malfunction, resulting in a backflow of blood into the heart.
The FDA is calling on parents not to feed Mother's Touch formula to infants, due to a lack of proper nutrients and a possible infection risk.
The FDA is warning that a form of heart surgery used to treat atrial fibrillation appears to carry greater health risks for women than men.
A new study suggests that a type of heart implant being investigated by the FDA is linked to an increased risk of blood clots.
The FDA is warning about a risk of heart problems, such as heart attacks and deaths, associated with Abbott's BVS dissolving heart implant.
Thousands of MitraClip heart surgery devices have been recalled following one patient death and a number of injuries caused by part of the device being left in the heart.
A lawsuit alleges side effects of AndroGel and Axiron caused the wrongful death of a Delaware man who was using the low T treatments.
The FDA warns that recalled Acclaim infusion pumps may cause overdoses or delay crucial medication therapy.