FDA continues its investigation of adverse event report related to French Lentil & Leek Crumbles

The FDA, CDC, and state and local partners continue investigating consumer complaints of gastrointestinal illness and abnormal liver function attributed to eating Daily Harvest French Lentil & Leek Crumbles frozen product. Daily Harvest voluntarily recalled the product on June 17, 2022. As of July 28, 2022, the FDA has received 329 Consumer Adverse Event Reports (CAERS) and Consumer Complaints related to this product in 36 states (AZ, CA, CO, CT, DE, FL, GA, IL, IN, IA, MD, MA, MN, MS, MI, MO, MT, NV, NH, NJ, NY, NC, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, and WI). The FDA does not provide a reason for the illnesses. @ https://www.fda.gov/food/outbreaks-foodborne-illness/investigation-adverse-event-reports-french-lentil-leek-crumbles-june-2022?utm_medium=email&utm_source=govdelivery