Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 15, 2019 (8 years ago)

Nita Crisp Spelt Bread Cracker recall

Recalled by Nita Foods Inc. · Fort Collins, CO, United States

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

Why it was recalled

Nita Crisp Spelt Bread Cracker for undeclared wheat.

Undeclared allergen: Wheat

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

Nita Crisp Spelt Bread Cracker, 8- & 16-ounce bags, In paper bags with a plastic window and has a re-closable ability and safety sealed. Storage: Ambient & Dry

Quantity: 210 cases

Food: Chips & snacks Bread & bakery

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.

October 11, 2018 through February 11, 2019 for Bar Code # 8-oz Spelt bags 88157620014 Bar Code # 16-oz Spelt bags 88157620021 Bar Code # 5-oz Spelt bags 88157620045 Bar Code # 2-oz Spelt cello packs 88157620038

Where it was sold

Nationwide.

California Colorado Idaho New Mexico Texas Utah Virginia

FDA's distribution note: Nation Wide ( Colorado, NM, UT, TX, ID, CA ). No foreign, VA, govt, military consignees.

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; 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
Nita Foods Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 15, 2019
In FDA report of
Mar 6, 2019
Terminated
Jul 25, 2019
FDA recall number
F-1100-2019 · event 82199
Official record
FDA enforcement report search

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