Class IITerminatedVoluntary: Firm initiated
Red Shell Foods, Inc.: food recall F-0696-2025
Red Shell Foods, Inc. of City Of Industry, CA recalled Teriyaki Sauce, Red Shell branded. Ingredients: Soy sauce(water, soybeans, wheat, salt, sodium benzoate), water,… Reason: Shelf stable Teriyaki sauce showing signs of micro growth (bubbling) and swelling containers. The FDA listed it as Class II in its Enforcement Report dated Apr 16, 2025; distribution: California.
Record status as published: Terminated (terminated Sep 19, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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)
- Product quantity
- 48 bottles (1 gallon size), 933 bottles (12 ounce size)
- Reason for recall
- Shelf stable Teriyaki sauce showing signs of micro growth (bubbling) and swelling containers.
- Codes, lots and dates on the package
- Lot: 120326 This is also the best by date printed on the container.
- Distribution pattern
- Primary direct account distribution is within California. Firm is currently working on distribution list information.
- Recalling firm
- Red Shell Foods, Inc., City Of Industry, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 17, 2025 |
| Classified by the FDA | Apr 8, 2025 |
| Published in the Enforcement Report | Apr 16, 2025 |
| Terminated | Sep 19, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0696-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.