Texamerican GF Turkey Chili 50 lbs. Item Number 1328903
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F1881-2015.
Texamerican Food Blending received notification from its supplier that two lots of ingredients were contaminated with Peanut allergen. The products affected do not have peanuts listed in the ingredient statement. All product items listed have a cleanout after mixing. The firm current corrective action in regard to receiving this ingredient is to discontinue ordering ingredient from Schiff Foo
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F1881-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Texamerican Food Blending, Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F1881-2015.
Texamerican Food Blending, Inc.
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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Texamerican Food Blending, Inc. Recall FAQ
Texamerican Food Blending, Inc. is the subject of a meat & poultry safety report: Texamerican GF Turkey Chili 50 lbs. Item Number 1328903. The notice was published on December 24, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 700 units are potentially affected.