Food Recall Check
Class I · High risk Terminated Initiated Jan 22, 2017 (10 years ago)

Trader Joe's Harvest Whole Wheat Bread recall

Recalled by Athens Baking Company · Fresno, CA, United States

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

Why it was recalled

Certain production dates of Trader Joe's Harvest Whole Wheat Bread do not declare cultured whey or list milk as an allergen.

Undeclared allergens: Milk 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

Trader Joe's Harvest Whole Wheat Bread; NET WT 24 oz. (1 lb. 8 oz.) SKU 00132; UPC: 0000 1328. Distributed and sold exclusively by: Trader Joe's, Monrovia, CA 91016

Quantity: 76410 units

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.

Best by Dates: 1/08/2017 through 1-27-2017. Code numbers: 364, 002, 004,005,006,010, 012,013,017.

Where it was sold

Arizona California New Mexico Nevada Utah

FDA's distribution note: AZ, CA, NV, NM, UT.

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 milk, 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
Athens Baking Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 22, 2017
In FDA report of
Mar 1, 2017
Terminated
Mar 30, 2017
FDA recall number
F-1525-2017 · event 76308
Official record
FDA enforcement report search

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