Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 16, 2019 (7 years ago)

Stop and Shop brand Grilled Salmon meal with cooked brown rice recall

Recalled by Taylor Farms New England, Inc. · North Kingstown, RI, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Salmon meals may contain undeclared wheat

Undeclared allergens: Wheat Fish

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

Stop and Shop brand Grilled Salmon meal with cooked brown rice, quinoa blend, broccoli florets, cooked white rice, fire roasted edamame, garlic and herb butter, bell pepper, roasted corn and carrots, Net Wt. 12.8 OZ (363g)

Quantity: 349 units total

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.

TFNE 350 Sell By 12/22/2019

Where it was sold

Massachusetts Maine New Jersey New York

FDA's distribution note: NJ, NY, MA, ME

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to wheat, fish; 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
Taylor Farms New England, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 16, 2019
In FDA report of
Jan 22, 2020
Terminated
Jul 20, 2020
FDA recall number
F-0503-2020 · event 84542
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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