Recall record at a glance
| Official record | H-0068-2025 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD |
| Report date | Jul 2, 2025 |
| Recall initiation date | May 6, 2025 |
| Quantity | 64,000 pounds (3200 cases) |
| Location | El Segundo, CA, United States |
Official product description
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
Why the product was recalled
Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites
Distribution information
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).
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Other.
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
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.