FDA recall record

Albertsons Companies Ready Meals Snow Crab Legs Imitation Surimi SCE NET WT 12 OZ recall — FDA F-0035-2023

Undeclared allergen; fish (anchovy)

Class IIclassification
F-0035-2023official record ID
Oct 19, 2022report date

Recall record at a glance

Official recordF-0035-2023
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAlbertsons Companies LLC
Report dateOct 19, 2022
Recall initiation dateAug 29, 2022
QuantityN/A
LocationBoise, ID, United States

Official product description

Ready 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

Why the product was recalled

Undeclared allergen; fish (anchovy)

Distribution information

U.S. distribution to the following: OR and WA No foreign distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.

Related recall records

Other records from the same recalling company are shown first when available.