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Lower risk Food recall · FDA · Published August 29, 2022

Albertsons Snow Crab Legs Recall: Undeclared Fish Allergen Risk

Albertsons recalls ready-to-eat snow crab legs due to undeclared fish (anchovy) allergen. Consumers should check product labels for ingredients and avoid if allergic to fish.

🇺🇸 FDA recall #F-0035-2023FoodAlbertsons ›
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Contact the company

Recalling firmAlbertsons Companies LLC250 E Park Center Blvd · Boise, ID 83726-0020
✎ GovInfoNow plain-language explainer

What happened, in plain English

Albertsons is recalling ready-to-eat snow crab legs that contain undeclared fish (anchovy) as an allergen. This poses a risk for people with fish allergies who might unknowingly consume the product. Read more at govinfonow.com/recall/12334-albertsons-snow-crab-legs-recall-undeclared-fish-allergen-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/12334-albertsons-snow-crab-legs-recall-undeclared-fish-allergen-risk · Updated August 18, 2026 · FDA enforcement record: FDA #F-0035-2023

Cite this page

“Albertsons Snow Crab Legs Recall: Undeclared Fish Allergen Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/12334-albertsons-snow-crab-legs-recall-undeclared-fish-allergen-risk. Based on FDA recall #F-0035-2023 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0035-2023%22&limit=1).

Why it’s dangerous

The product contains undeclared fish (anchovy) as an allergen. People with fish allergies could experience allergic reactions if they consume the product without knowing it contains fish.

Who’s affected

People with fish allergies, especially those sensitive to anchovies, are at risk from this recall. The product is sold in Albertsons and Safeway stores.

How to tell if you have this one

Check for the product name 'Ready Meals Snow Crab Legs Imitation Surimi' with UPC 0234639 306008. The recall covers items sold in Albertsons and Safeway stores up to and including September 1.

  • Brand
    Albertsons
  • Product
    Ready Meals Snow Crab Legs Imitation Surimi SCE NET WT 12 OZ CAL 300 NET WT. 0lb 12oz (340g) ready2eat Ingredients
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Status
    Terminated
  • Distribution
    U.S. distribution to the following: OR and WA No foreign distribution.
Recall numberProduct, codes & lotsClass
F-0034-2023Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Ingredients: Shrimp (Litopenaues Viannamei), Lemon, Salt, Tomato Paste, Sodium Tripolyphosphate (to retain moisture), water, high fructose corn syrup, contains 2% or less Beet Powder, Calcium, Disodium EDTA used to protect quality, Distilled Vinegar, Horseradish, Lemon Juice Concentrate, Natural and Artifical Flavor, Potassium Sorbate, Sodium Benzoate (Used as Preservatives), Soybean Oil, Xanthan Gum **Contains: Soy and Crustacean (Shrimp)** Perishable-Keep Refrigerated UPC 0234638 306009 Dist by: Safeway Inc. Pleasanton CA 94588 Store Banners: Albertsons and Safeway; All Sell Thru Dates up to and including Sept. 1Class I
F-0035-2023Ready Meals Snow Crab Legs Imitation Surimi SCE NET WT 12 OZ CAL 300 NET WT. 0lb 12oz (340g) ready2eat Ingredients: Fish Protein (one or more Pollock, Pacific Whiting), Water, Lemon, Tomato Paste, What Starch, High Fructose Corn Syrup, Sugar, Egg Whites, Sorbitol, Crabmeat (Chionoecetes Opilio, Chionoecetes Bairoil, Chionoecetes Japonicus), Contains 2% or Less Artificial Flavors, Beet Powder, Brown Rice Syrup, Calcium Disodium EDTA Use to Protect Quality, Canola Oil, Carmine & Paprika For Color, Distilled Vinegar, Glycerin, Horseradish, Hydrolyzed Gelatin, Lemon Juice Concentrate, Mirin (Rice Wine), Natural and Artificial Flavor, Potassium Sorbate, Sodium Benzoate (Used as Preservatives), Salt, Sodium Tripolyphosphate, Soy Lecithin, Soybean Oil, Tapioca Starch, Tetrasodium Pyrophosphate, Whole Egg, Xanthan Gum **Contains: Egg, Soy, Wheat, Crustacean (Crab) and FIsh (Pollock, Whiting)** Perishable-Keep Refrigerated UPC 0234639 306008 Dist by: Safeway Inc. Pleasanton CA 94588 Store Banners: Albertsons and Safeway; All Sell Thru Dates up to and including Sept. 1Class II
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the ingredient list that lists 'Fish (Pollock, Whiting)' or 'Crustacean (Crab)' and check for the UPC 0234639 306008.

Where it went and when

Where it was distributed

Distributed in Oregon and Washington.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “U.S. distribution to the following: OR and WA No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Oregon, Washington.

Recall timeline

FDA terminated this recall 52 days after the firm started it.

1. Firm started the recall: Aug 29, 202212. FDA classified it Class II: Oct 7, 202223. Published in FDA’s Enforcement Report: Oct 19, 202234. FDA terminated the recall: Oct 20, 202242022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0035-2023 (August 29, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0035-2023 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA