Class ITerminatedVoluntary: Firm initiated
TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD: food recall H-0068-2025
TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD of El Segundo, CA recalled Frozen Shrimp- packaged in 5lb frozen IQF blocks/4 blocks to a case. Unlabeled generic case packaging reads: "Raw P&D… Reason: Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites. The FDA listed it as Class I in its Enforcement Report dated Jul 2, 2025.
Record status as published: Terminated (terminated Jul 1, 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
- Frozen Shrimp- packaged in 5lb frozen IQF blocks/4 blocks to a case. Unlabeled generic case packaging reads: "Raw P&D Tail-On White Shrimp" 26/30; Contains: Shrimp (Crustacean) UPC# 1 08432370 0405 5
- Product quantity
- 64,000 pounds (3200 cases)
- Reason for recall
- Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites
- Codes, lots and dates on the package
- Lot# 669/18WH/124; 669/19WH/134; 669/20WH144; 669/30VH/127; 669/01HH/003; 669/03HH011 Best BY: Jul 18, 2026; Jul 19, 2026; Jul 20,2026; Sep 30,2026; Oct 01,2026; Oct 03,2026
- Distribution pattern
- Affected lots were sold exclusively to Whole Foods USA. Whole Foods uses some of the product for its retail in-store deli. Product was distributed to various Whole Foods stores across the country. The remaining portion of the lot, is passed through to a downstream customer in Canada (Seven Seas Fish Co. LTD).
- Recalling firm
- TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD, El Segundo, CA
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Other
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 6, 2025 |
| Classified by the FDA | Jun 24, 2025 |
| Published in the Enforcement Report | Jul 2, 2025 |
| Terminated | Jul 1, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0068-2025 (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.