Friday, August 5, 2022

Outbreak Case Counts Increase for Daily Harvest's Lentil and Leek Crumbles, Tara Flour Identified as Cause

As last reported by FDA on 7/28/22 on a disease outbreak associated with Daily Harvest's Lentil and Leeks Crumble, there have been 329 illness events with 113 hospitalized.  The cause of the outbreak has been identified as the Tara Flour, but there is little more information than that.

Case Counts
Total Adverse Illness Events: 329*
Hospitalizations: 113*
Deaths: 0
Last illness onset: July 16, 2022*
States with Adverse Illness Events: 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, WI
Product Distribution: Nationwide
*Estimate based on Consumer Complaint and CAERs reports received by the FDA


https://www.fda.gov/food/outbreaks-foodborne-illness/investigation-adverse-event-reports-french-lentil-leek-crumbles-june-2022?utm_medium=email&utm_source=govdelivery#contact
Investigation of Adverse Event Reports: French Lentil & Leek Crumbles (June 2022)

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

The FDA, along with CDC and state and local partners, is investigating consumer complaints of gastrointestinal illness and abnormal liver function that may be attributable to eating Daily Harvest French Lentil & Leek Crumbles frozen product.

On June 17, 2022, in response to consumer complaints submitted to the company, Daily Harvest voluntarily initiated a recall of their French Lentil & Leek Crumbles. In response to Consumer Adverse Event Reports (CAERS) and Consumer Complaints submitted to the FDA, the FDA has initiated an investigation, including an inspection and sample collection in an effort to determine the cause of illnesses. As of July 28, 2022, the FDA has received 329 CAERS reports and Consumer Complaints related to this product.

FDA’s investigation is ongoing, and more information will be provided as it becomes available.
July 14, 2022

The FDA, along with CDC and state and local partners, is investigating consumer complaints of gastrointestinal illness and abnormal liver function that may be attributable to eating Daily Harvest French Lentil & Leek Crumbles frozen product.

On June 17, 2022, in response to consumer complaints submitted to the company, Daily Harvest voluntarily initiated a recall of their French Lentil & Leek Crumbles. In response to Consumer Adverse Event Reports (CAERS) and Consumer Complaints submitted to the FDA, the FDA has initiated an investigation, including an inspection and sample collection in an effort to determine the cause of illnesses. As of July 14, 2022, the FDA has received 277 CAERS reports and Consumer Complaints related to this product.

FDA’s investigation is ongoing, and more information will be provided as it becomes available.


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