Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 7, 2017 (10 years ago)

Midwest Northern Nut Cajun Cracker Mix recall

Recalled by Midwest Northern Inc · Minneapolis, MN, United States

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

Why it was recalled

potential Allergen cross contact in oil used to roast various nuts and seeds products.

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

Midwest Northern Nut Cajun Cracker Mix, Snack Mix. Packaged in the following sizes: 1. Net Wt. 16 oz. (454G), UPC 38043-90032. 2. Net Wt. 5 lbs. 3. Net Wt. 20 lbs. 4. Net Wt. 25 lbs. Midwest Northern Inc., Minneapolis, MN 55118

Quantity: 35,056 lbs. total

Food: Chips & snacks

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 Numbers: 002180 - 061180

Where it was sold

Alaska Georgia Iowa Indiana Kentucky Minnesota Missouri North Dakota New Hampshire New York Ohio Texas Wisconsin

FDA's distribution note: AK, GA, IA, IN, KY, MN, MO, ND, NH, NY, OH, TX, WI

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. 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
Midwest Northern Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 7, 2017
In FDA report of
Apr 25, 2018
Terminated
Apr 25, 2018
FDA recall number
F-1051-2018 · event 79458
Official record
FDA enforcement report search

Also recalled with it (65 more products)

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

Showing 12 of 65.