Update on the investigation of French Lentil & Leek Crumbles

The FDA reported that as of August 25, 2022, they received 369 Consumer Adverse Event Reports (CAERS) related to the French Lentil & Leek Crumbles. There have been 125 hospitalizations due to the product. States with Adverse Illness Events: AZ, CA, CO, CT, DE, FL, GA, IL, IN, IA, KS, 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. @ https://www.fda.gov/food/outbreaks-foodborne-illness/investigation-adverse-event-reports-french-lentil-leek-crumbles-june-2022?utm_medium=email&utm_source=govdelivery

 

 Investigation of Adverse Event Reports: French Lentil & Leek Crumbles
Investigation of Adverse Event Reports: French Lentil & Leek Crumbles

Do not eat, sell, or serve recalled French Lentil & Leek Crumbles from Daily Harvest. FDA’s investigation is ongoing.

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