Regulatory

Over the past year and a half, Jeni’s Splendid Ice Cream has struggled with the presence of Listeria monocytogenes in its production facility. Despite taking extensive precautions, a Food and Drug Administration (FDA) warning letter released today indicates that eradication efforts have failed.

This week natural products retailer Whole Foods Market received a warning letter from the FDA for numerous “serious violations” of the U.S. Food and Drug Administration’s (FDA) Current Good Manufacturing Practice (cGMP) regulations for manufacturing, packing or holding food.

First Lady Michelle Obama – who has played an active role in efforts to update the Nutrition Facts panel since 2014 – said the label changes “make a real difference in providing families across the country information they need to make healthy choices.”

Any food or beverage company will tell you that the day a Food and Drug Agency (FDA) warning letter shows up in the mail is, in the politest terms, nerve-wracking. But it seems you can sometimes fight City Hall. Despite what some believe is pressure from Big Food to keep with the status quo, it seems the FDA has realized it needs to start pulling some of its punches in the case of certain claims or claims used for specific functions.

The U.S. Department of Agriculture and the Department of Health and Human Services released their final draft of the nation’s federal dietary guidelines yesterday. Since then numerous industry groups and companies have issues statements lauding or disagreeing with the new guide.

The Food and Drug Association has extended the comment period for use of the term “Natural.” by 90 days. Originally comments were due February 10th, but now have been moved to May 10th.

In addition to the FDA’s announcement regarding the approval of genetically modified salmon, the agency also released suggestions for those companies that want to voluntarily call attention to the fact that they are using genetically modified (GMO) ingredients (of the aquatic nature or otherwise).

In an effort to improve the labeling requirements of certain gluten-free products, the U.S. Food and Drug Administration has proposed new rules on the designation for producers of fermented, distilled or hydrolyzed foods.

Recent articles published by The Guardian and the Associated Press reported that members of the American Egg Board, a government-backed lobbying group, engaged in a long-running campaign intended to debilitate sales and distribution growth of Hampton Creek’s Just Mayo, a product that is formulated without eggs.

What do you do when your signature product’s name is deemed unacceptable by the U.S. Food and Drug Administration (FDA)? That’s the situation Hampton Creek is in after the government agency sent a warning letter to the company regarding its Just Mayo brand.