Recall record at a glance
| Official record | F-2199-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Corn Maiden Foods |
| Report date | May 20, 2015 |
| Recall initiation date | Apr 14, 2015 |
| Quantity | 254 cases (3 x8lbs/case) |
| Location | Harbor City, CA, United States |
Official product description
Border Grill Tortilla Soup Item # BOR-010, 3 x 8 lbs bags/case with Lot Codes Numbers between 140409 and 150311 Corn Maiden Foods, Inc. 24201 Frampton Av. Harbor City, CA 90710 LOT # Expiration Date Frozen: Expiration After Thaw: 7 days Border Grill Tortilla Soup INGREDIENTS: Sauce: Water, tomato filets (tomatoes, salt, calcium, chloride, citric acid), fresh tomatoes, onion, garlic, jalapeno chile, chicken base (chicken meat including natural chicken juices, natural sea salt, chicken fat, vegetable extract (potato, carrot, onion), yeast extract, tumeric, natural flavors), Kosher salt, olive oil blend (olive oil, canola oil), chipotle chile, black pepper. COUNTAINS THE FOLLOWING ALLERGENS: NONE KEEP FROZEN OR REFRIGERATED 3 Bags x 8 lbs/Case Net Weights 24 lbs.
Why the product was recalled
The firm is recalling Border Grill Tortilla soup due to the product having undeclared hydrolyzed soy protein that is a sub-ingredient in the ingredient; chicken base.
Distribution information
One customer (restaurant) in Los Angeles, CA
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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