Ready Meals Snow Crab Legs Imitation Surimi SCE NET WT 12 OZ CAL 300 NET WT. 0lb 12oz (340g) ready2eat Ingredients: Fi
Summary
The FDA issued a Class II for Ready Meals Snow Crab Legs Imitation Surimi SCE NET WT 12 OZ CAL 300 NET WT. 0lb by Albertsons Companies LLC. Reason: Undeclared allergen; fish (anchovy).
Details
Source
Food Recall
External ID
F-0035-2023
Action Date
2022-10-19
Status
Terminated
Category
food
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
Lot/Code Info: All Sell Thru Dates up to and including Sept. 1
Quantity Affected: N/A
Reason for Recall
Undeclared allergen; fish (anchovy)
Distribution
U.S. distribution to the following: OR and WA No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-08-29
Company
Boise, ID
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Albertsons Companies LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Albertsons Companies LLC have FDA actions?
Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0035-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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