Pico De Gallo
Reason Potential contamination with Salmonella.
Teriyaki Sauce Red Shell branded recall
Recalled by Red Shell Foods, Inc. · City Of Industry, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Shelf stable Teriyaki sauce showing signs of micro growth (bubbling) and swelling containers.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Teriyaki Sauce, Red Shell branded. Ingredients: Soy sauce(water, soybeans, wheat, salt, sodium benzoate), water, sugar, cooking wine( water, rice, malt), sweet cooking wine(corn syrup, rice, water, malt), modified food starch, dried onion, dried ginger root, dried garlic, lactic acid, spices. "Shake well before use. Keep Refrigerated after opening" UPC# 0-18529-10001-9 (12 ounce) UPC# 0-18529-10505-6 (1 gallon)
Quantity: 48 bottles (1 gallon size), 933 bottles (12 ounce size)
Food: Sauces, dips & dressings
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot: 120326 This is also the best by date printed on the container.
Where it was sold
California
FDA's distribution note: Primary direct account distribution is within California. Firm is currently working on distribution list information.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Red Shell Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 17, 2025
- In FDA report of
- Apr 16, 2025
- Terminated
- Sep 19, 2025
- FDA recall number
- F-0696-2025 · event 96540
- Official record
- FDA enforcement report search
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