Class ITerminated in FDA datasetRecall initiated Aug 29, 2022

Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g)…

Recalling firm: Albertsons Companies LLC

Why it was recalled

Undeclared allergen; fish (anchovy)

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 20, 2022.

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ProductReady 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
Package size12 OZ

FDA code information

All Sell Thru Dates up to and including Sept. 1

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Full FDA record and distribution details

Original product description

Ready 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

Original FDA recall reason

Undeclared allergen; fish (anchovy)

Recall details

Recall number
F-0034-2023
Event ID
90829
FDA status
Terminated
Initiated
Aug 29, 2022
Reported
Oct 19, 2022
Classified
Oct 7, 2022
Terminated
Oct 20, 2022
Quantity
N/A
Location
Boise, ID, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

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

FDA source record · F-0034-2023

Data updated September 16, 2026. View official FDA data ↗

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