Food Recall Check
Class III · Low risk Terminated Initiated Nov 8, 2025 (11 months ago)

Pacific Seafood Raw Blackened Shrimp Peeled & Deveined Tail-Off recall

Recalled by Pacific Seafood - Portland, LLC · Clackamas, OR, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Undeclared Sulfite. Shrimp may contain 3.4mg Sulfur Dioxide per serving and label does not declare Sulfite.

Undeclared allergen: Shellfish

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Pacific Seafood Raw Blackened Shrimp Peeled & Deveined Tail-Off, refrigerated, farm-raised. Net wt. per tray 8 oz (227 g). UPC 0 27241 44630 5. Ingredients: Shrimp (Shrimp, Water, Salt, Sodium tripolyphosphate (to retain moisture), Blackened Seasoning (Sea Salt, Paprika, Spices, Onion, Garlic, Paprika Extract). CONTAINS: Shrimp (Crustacean Shellfish). Product of Ecuador. Packed and distributed by Pacific Seafood Group Clackamas, OR.

Quantity: Total of 15,498 lbs.

Food: Seafood & fish

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 Numbers: 4211281; 4210119; 4209823

Where it was sold

Alabama Florida Massachusetts

FDA's distribution note: Distributed in AL, FL, and MA.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to shellfish; for anyone else the product is generally not a safety concern. 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
Pacific Seafood - Portland, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 8, 2025
In FDA report of
Dec 10, 2025
Terminated
Jan 26, 2026
FDA recall number
H-0226-2026 · event 97963
Official record
FDA enforcement report search

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