Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 7, 2014 (13 years ago)

Simply balanced herb mixed freeze dried vegetables all natural recall

Recalled by American Importing Co, Inc · Minneapolis, MN, United States

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

Why it was recalled

Amport Foods is recalling a limited amount of Target Simply Balanced Herb Mixed Freeze Dried Vegetable due to a potential for undeclared soy.

Undeclared allergen: Soy

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

Simply balanced, herb mixed freeze dried vegetables all natural, Ingredients: Super sweet corn, edamame, peas, carrots, (carrots, sugar, dextrose, tapioca starch), Italian seasoning (Garlic, tomato (tomato, salt), crushed red pepper, basil, oregano), coconut oil, sea salt. May contain peanut, tree nuts, milk, soy, and wheat., Net WT 2.5 oz (71 g), UPC 0 85239 08318 5, distributed by Target Corporation, Minneapolis, MN 55403.

Quantity: 2,288 cases (12/case)

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.

Lot #: 205X317, 213X317, 253X317. Best By: 24JUL14; 01AUG14; 10SEPT14

Where it was sold

Minnesota

FDA's distribution note: MN

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 soy; 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
American Importing Co, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 7, 2014
In FDA report of
Feb 5, 2014
Terminated
Jul 13, 2017
FDA recall number
F-1443-2014 · event 67229
Official record
FDA enforcement report search

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