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

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

Class II recalls from the FDA indicate a potential risk to consumer safety where use or exposure to the product may cause ...

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

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 ...

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

Exactly a year after the brand's historically large lunch meat recall comes a report about an issue with another mainstream ...

When recalls go out to the public, consumers can often return the product for a refund, or they are advised to safely dispose of it. There are a slew of reasons why a product could be recalled ...

The results explain the reason behind the recall, where the drug was distributed, the nature of the recall and the manufacturer's country of origin.

FDA issues 19 recalls in August for food, drinks. The U.S. Food and Drug Administration issued 19 recalls in August for various food and beverages. While not all of them were sold in Florida, here ...

When the FDA recalls a product, there are several different categories it could fall into. As a consumer, it is important to be mindful or recalls to ensure you take the proper precautions.

The trend may, in part, be a holdover from the height of the COVID-19 pandemic, when fewer than 4,000 FDA inspections of food-producing facilities were done in the U.S., compared to more than ...