Country Harvest brand Black Thunder Bean Soup, dried soup mix is packaged in poly pro bag, heat sealed and placed in another poly pro bag & tape sealed. Net. 8 oz. UPC 7 29818 00104 6. The label is read in parts" ***For That Home Cooked Goodness***Country HARVEST ***BLACK THUNDER BEAN SOUP***INGREDIENTS***Blackbeans, onion, chicken soup base (salt, maltodextrine, dextrose, dairy whey***".

Class I - Dangerous
Recalled: September 14, 2017 Country Harvest Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Best By dates: 10/1/2017 to 8/31/2019
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Country Harvest, Inc.
Reason for Recall:
Country Harvest brand Black Thunder Bean Soup is recalled because the ingredients statement declared Dairy Whey but did not declare milk.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Country Harvest brand Black Thunder Bean Soup, dried soup mix is packaged in poly pro bag, heat sealed and placed in another poly pro bag & tape sealed. Net. 8 oz. UPC 7 29818 00104 6. The label is read in parts" ***For That Home Cooked Goodness***Country HARVEST ***BLACK THUNDER BEAN SOUP***INGREDIENTS***Blackbeans, onion, chicken soup base (salt, maltodextrine, dextrose, dairy whey***".

Product Codes/Lot Numbers:

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

Distribution:

Distributed in: AK, CA, ID, NM, OK, OR, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0002-2018

Related Recalls