Food Recall Check
Class I · High risk Terminated Initiated Dec 19, 2012 (14 years ago)

Udi's gluten free au naturel granola in recall

Recalled by Udi's Healthy Foods,Granola & Gluten Free · Denver, CO, United States

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

Why it was recalled

Product may contain undeclared almonds.

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

Udi's gluten free au naturel granola in 12 ounce clear plastic bag, UPC 6-98997-80615-8, best by 041913 12265 1.

Quantity: 3510 - 12 ounce bags shipped (585 cases)

Food: Pasta, rice & grains

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.

UPC 6-98997-80615-8 Best by 041913 122565 1

Where it was sold

California Colorado Idaho Montana Nevada Oregon Utah Washington

FDA's distribution note: US Distribution: 5 direct accounts in WA, CA, CO with subaccount distribution to WA, CA, CO, NV, UT, MT, ID, and OR.

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. 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
Udi's Healthy Foods,Granola & Gluten Free
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 19, 2012
In FDA report of
Jan 16, 2013
Terminated
Apr 11, 2013
FDA recall number
F-0864-2013 · event 63928
Official record
FDA enforcement report search

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