The FDA plays a crucial role in safeguarding public health by monitoring the safety of products. Recently, two significant ...

Recent actions by the Food and Drug Administration (FDA or Agency) reflect a sharpened scrutiny in areas where public health and safety may ...

Ten different flavors, coming from a brand sold through one classic summertime method, are reportedly impacted.

Sandoz has issued a nationwide recall of two lots of cefazolin for injection due to a labeling error. The mislabeled vials were sent to wholesalers for nationwide distribution.  The error was found ...

Dexcom (Nasdaq:DXCM) has issued an update related to a recall for its continuous glucose monitor (CGM) components.

More than 67,000 cases of a popular deodorant brand sold by retailers nationwide were recalled due to an undisclosed ...

More than 67,000 cases of Power Stick antiperspirant deodorant sold nationwide have been voluntarily recalled due to manufacturing issues.

An enforcement report from the Food and Drug Administration revealed that more than 67,000 cases of Power Stick deodorant have been recalled.

The next time you roll on your deodorant while getting ready for a steamy summer day, check the label—it may be unsafe to use ...

Check the label on your deodorant ASAP. Tens of thousands of cases of Power Stick antiperspirant deodorant have been recalled ...

WASHINGTON - A.P. Deauville, LLC, has voluntarily recalled more than 67,000 cases of various Power Stick roll-on ...

As such, the FDA has classified the New Mexico Pinon Coffee pod recall as a Class III risk. The FDA defines such a risk as “a ...