Food Recall Check
Class I · High risk Terminated Initiated Dec 28, 2012 (14 years ago)

Kinnikinnick Pie Crust Gluten Free recall

Recalled by United National Foods (Unfi) · Aurora, CO, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

UNFI Aurora, Colorado is recalling certain Kinnikinnick Pie Crusts (frozen) because they were notified by the manufacturer, Kinnikinnick Foods (Alberta, Canada) that the products contain eggs and are not identified in the finished product labeling.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Kinnikinnick Pie Crust Gluten Free (frozen) weight 290 g/ 10 oz Qty/Pkg: 2, UPC 620133006229, Kinnikinnick Foods 10940 120 Street, Edmonton, AB Canada.

Quantity: 877 x 10 oz packages

Food: 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.

US distribution: BB2013NO30; BB2013DE12; BB2013DE13; BB2013DE14; BB2013DE17; BB2013DE04; BB2013DE11; BB2013NO28; BB2013NO29; BB2013NO23; BB2013DE06; BB2013DE05; BB2013NO28; BB2013NO19; BB2013DE04; BB2013NO27.

Where it was sold

California Colorado Texas Washington

FDA's distribution note: Distributed to UNFI distribution centers located in WA, CA, CO, and TX.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
United National Foods (Unfi)
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 28, 2012
In FDA report of
Jan 16, 2013
Terminated
Apr 15, 2013
FDA recall number
F-0865-2013 · event 63998
Official record
FDA enforcement report search

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