The Food and Drug Administration (FDA) has issued a recall for Golden Crop Candy sold in eight states, including New York. The recall was initiated by Blooming Import Inc. in Brooklyn after the ...

The FDA classified the recall as a Class II Below, find a list of impacted products. Check your medicine cabinets: More than 7,000 bottles of Multi-V Men daily multivitamins are being recalled.

Duda Farm Fresh Foods, Inc. is recalling its Marketside Celery Sticks over listeria concerns. The U.S. Food and Drug Administration issued an alert, advising customers to immediately discontinue ...

Many Texans love an ice-cold Coca-Cola, but a recent recall from the U.S. Food and Drug Administration may concern consumers. The FDA recalled 864 12-packs of Coca-Cola sold in two states ...

When you learn about a recall involving an FDA-regulated product that you or a loved one has purchased or used, there are several pieces of information you need in order to make informed decisions ...

Just when you thought things couldn't get any worse, the FDA swoops in and recalls almost a ton of butter. All Recipes is reporting that the U.S. Food & Drug Administration has announced a recall ...

Those with an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the recalled product, according to the FDA recall report.

On April 15, the recalled chocolate bars were given a Class II recall classification by the FDA, indicating that the chocolate bars “may cause temporary or medically reversible adverse health ...

It can feel like a job just keeping up with what the FDA informs the public of when foods and drugs are removed from grocery stores and pharmacies. Here is what we know about what food and drugs ...

The FDA recalled over 4,000 bags of ground coffee mislabeled as decaffeinated across 15 states. The recall applies to 12-ounce bags of Our Family's Traverse City Cherry Decaf Light Roast.

cans on March 6. On Monday, March 24, the U.S. Food and Drug Administration (FDA) classified it as a Class II recall, meaning that the risk is remote. 864 units of 12-packs, meaning more than ...