Two weeks after the company began receiving reports of liver failure the FDA has announced it is investigating an outbreak of “adverse reactions” to Daily Harvest brand French Lentil & Leek Crumbles.

As of June 28 the Food and Drug Administration had received at least 133 reports of what it calls adverse events from consumers who ate the frozen crumbles product, according to an announcement this afternoon. The implicated product was shipped nationwide.

The company recalled the product on June 17 after receiving complaints from consumers of gastrointestinal illnesses and abnormal liver function. Some patients also reported having to have

Continue Reading FDA officially names Daily Harvest crumbles as being under investigation for illnesses