A recall of infants' oral drops made by the Perrigo Co. has been announced by The Food and Drug Administration (FDA).

In a news release Monday, the FDA said the drops come with a syringe that could make it confusing for parents to give their children the proper dose, leading to overdose

The Food and Drug Administration gives conditional approval for controversial silicone breast implants by Mentor Corp.

The FDA requires the company to satisfy a number of conditions before it receives final approval to sell the silicone gel-filled implants. The conditions were "generally consistent" with recommendations from an expert panel that met earlier this year

The FDA is approved a first-of-its-kind implantable electrical nerve stimulator device to treat severe depression.

The Vagus Nerve Stimulation (VNS) System is approved for adult patients with long-term or recurrent major depression that has not responded properly to four or more antidepressant treatments

The FDA is approved a first-of-its-kind implantable electrical nerve stimulator device to treat severe depression.

The Vagus Nerve Stimulation (VNS) System is approved for adult patients with long-term or recurrent major depression that has not responded properly to four or more antidepressant treatments

The FDA is approved a first-of-its-kind implantable electrical nerve stimulator device to treat severe depression.

The Vagus Nerve Stimulation (VNS) System is approved for adult patients with long-term or recurrent major depression that has not responded properly to four or more antidepressant treatments