CLASS II Food recall · Reported 15 Mar 2023 · FDA Enforcement Report
French Lentil + leek Crumbles recalled by Daily Harvest
Daily Harvest is recalling French Lentil + leek Crumbles, distributed nationwide in the US. The recall was initiated on 17 Jun 2022 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0419-2023
- FDA event ID
- 90474
- Recalling firm
- Daily Harvest, New York, NY
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 17 Jun 2022
- FDA classified
- 9 Mar 2023
- Reported
- 15 Mar 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Temperature Abuse
- Product category
- Beans & Lentils
Timeline
| 17 Jun 2022 | Recall initiated by company | |
| 9 Mar 2023 | Classified by FDA | +265 days |
| 15 Mar 2023 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product is linked to complaints of gastrointestinal illness.
Foods that need refrigeration and were stored or shipped too warm can grow harmful bacteria without any change in look or smell.
Product as listed by the FDA
Daily Harvest French Lentil + leek Crumbles, Item ID L02-VEGBN, Net Wt. 12 oz. (340g) Keep Frozen, Cook Thoroughly. Perishable. Store Frozen. Cook Thoroughly to internal temperature of 165F. Distr. by Daily Harvest Inc. New York, NY 10013.
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Product is linked to complaints of gastrointestinal illness.
Which lots are affected?
Lot Codes: 9/27/2022 L5-A, 10/10/2022 L5-A, 10/23/2022 L5-A, 11/6/2022 L5-A, 11/14/2022 L5-A, 11/15/2022 L5-A
Where was it sold?
Nationwide
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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