DAILY HARVEST Recall: Product is linked to complaints of gastrointestinal illness.
United States
TerminatedClass II
- Company
- DAILY HARVEST
- Product
- Daily Harvest French Lentil + leek Crumbles, Item ID L02-VEG…
- Recall date
- June 17, 2022
- Terminated
- April 3, 2025
- Source
- FDA
Reason for recall
Product is linked to complaints of gastrointestinal illness.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | Not published in this source record | 28,776 units | 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 |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0419-2023
- Event ID
- 90474
- Status
- Terminated
- Classification
- Class II
- Company
- DAILY HARVEST
- Product description
- 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.
- Quantity
- 28,776 units
- Reason
- Product is linked to complaints of gastrointestinal illness.
- Recall initiation date
- June 17, 2022
- Report date
- March 15, 2023
- Classification date
- Not published in this source record
- Termination date
- April 3, 2025
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- 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
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: DAILY HARVEST
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
