FDA Recall United States Terminated Historical recordClass II
Country Harvest, Inc.
- Product
- Country Harvest brand Black Thunder Bean Soup, dried soup mi…
- Published
- October 11, 2017
- Distribution
- distributed in AK, CA, ID, NM, OK, OR, W…
Country Harvest, Inc. Recall: Country Harvest brand Lentil Barley Soup is recalled because the ingredients statement declared Dairy Whey but did not declare milk.
United States
TerminatedClass II
- Company
- Country Harvest, Inc.
- Product
- Country Harvest brand Lentil Barley Soup, dried soup mix is…
- Recall date
- September 14, 2017
- Terminated
- November 13, 2017
- Source
- FDA
Reason for recall
Country Harvest brand Lentil Barley Soup is recalled because the ingredients statement declared Dairy Whey but did not declare milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Country Harvest brand Lentil Barley Soup, dried soup mix is packaged in poly pro bag, heat sealed and placed in another poly pro bag & tape sealed. Net wt. 7 oz. UPC 7 29818 00103 9. The label is read in parts" ***For That Home Cooked Goodness***Country HARVEST ***LENTIL BARLEY SOUP***INGREDIENTS***Lentils, barley, onions, beef soup base ***vegetable shortening ***corn starch*** dairy whey***". | Not published in this source record | approximately 1700/7 oz. packages | Best By dates: 10/1/2017 to 8/31/2019 |
Distribution
- distributed in AK
- CA
- ID
- NM
- OK
- OR
- WA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0003-2018
- Event ID
- 78119
- Status
- Terminated
- Classification
- Class II
- Company
- Country Harvest, Inc.
- Product description
- Country Harvest brand Lentil Barley Soup, dried soup mix is packaged in poly pro bag, heat sealed and placed in another poly pro bag & tape sealed. Net wt. 7 oz. UPC 7 29818 00103 9. The label is read in parts" ***For That Home Cooked Goodness***Country HARVEST ***LENTIL BARLEY SOUP***INGREDIENTS***Lentils, barley, onions, beef soup base ***vegetable shortening ***corn starch*** dairy whey***".
- Quantity
- approximately 1700/7 oz. packages
- Reason
- Country Harvest brand Lentil Barley Soup is recalled because the ingredients statement declared Dairy Whey but did not declare milk.
- Recall initiation date
- September 14, 2017
- Report date
- October 11, 2017
- Classification date
- Not published in this source record
- Termination date
- November 13, 2017
- Distribution pattern
- distributed in AK, CA, ID, NM, OK, OR, WA
- UPC, lot, and code information
- Best By dates: 10/1/2017 to 8/31/2019
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 78119 with 1 other product entry in Public Health Trace.
Responsible company: Country Harvest, Inc.
Other recalls from Country Harvest, Inc.
FDA Recall United States Terminated Historical recordClass II
Country Harvest, Inc.
- Product
- Country Harvest brand Black Thunder Bean Soup, dried soup mi…
- Published
- October 11, 2017
- Distribution
- distributed in AK, CA, ID, NM, OK, OR, W…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alaska | 1 |
| California | 1 |
| Idaho | 1 |
| New Mexico | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Washington | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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.
