Class IITerminated in FDA datasetRecall initiated Sep 14, 2017

Country Harvest brand Lentil Barley Soup, dried soup mix is packaged in poly pro bag, heat…

Recalling firm: Country Harvest, Inc.

Why it was recalled

Country Harvest brand Lentil Barley Soup is recalled because the ingredients statement declared Dairy Whey but did not declare milk.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 13, 2017.

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ProductCountry 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***".
Package size7 oz
UPC729818001039

FDA code information

Best By dates: 10/1/2017 to 8/31/2019

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Full FDA record and distribution details

Original 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***".

Extracted codes and context

TypeCode / valueContext
UPC729818001039eat 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*

Original FDA recall reason

Country Harvest brand Lentil Barley Soup is recalled because the ingredients statement declared Dairy Whey but did not declare milk.

Recall details

Recall number
F-0003-2018
Event ID
78119
FDA status
Terminated
Initiated
Sep 14, 2017
Reported
Oct 11, 2017
Classified
Oct 3, 2017
Terminated
Nov 13, 2017
Quantity
approximately 1700/7 oz. packages
Location
Spokane, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed in AK, CA, ID, NM, OK, OR, WA

FDA source record · F-0003-2018

Data updated September 16, 2026. View official FDA data ↗

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