Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 10, 2022 (4 years ago)

Nick's Krispi Nougat Protein Bar recall

Recalled by Luthman Backlund Foods USA INC · El Segundo, CA, United States

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

Why it was recalled

Nick's Krispi Nougat Protein Bar is being recalled due to containing hazelnuts, which is not declared on the label.

Undeclared allergen: Tree nuts

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

Nick's Krispi Nougat Protein Bar, 1.76 oz., in foil wrapper in 12 pack boxes. UPC: 00850009682345 Product of North Macedonia Distributed by LUB Foods USA, Inc. El Segundo, CA 90245

Quantity: 61, 016 bars

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.

Expiration Date: 07/20/2023 - Lot Codes: L2406 and L2506

Where it was sold

Arizona California Georgia Massachusetts Maryland North Carolina New York Oregon Pennsylvania Texas Vermont Washington

FDA's distribution note: Firm has 15 consignees located in OR, AZ, CA, GA, MD, TX, NC, PA, VT, NY, MA, and WA

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 tree nuts; 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
Luthman Backlund Foods USA INC
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 10, 2022
In FDA report of
Oct 26, 2022
Terminated
Jan 24, 2023
FDA recall number
F-0046-2023 · event 90991
Official record
FDA enforcement report search