Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 12, 2012 (14 years ago)

E-3 Seasoning/Spice recall

Recalled by Boyd Coffee Co · Portland, OR, United States

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

Why it was recalled

sub-ingredients hydrolyzed soy protein and hydrogenated soybean oil were not declared on the finished product label of E-3 Seasoning.

Undeclared allergen: Soy

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

E-3 Seasoning/Spice, Part #1690. Product is packaged in a white bucket. Net weight 35 lbs. The product is labeled in parts: "***E-3 SEASONING***NET WT 35 LB***Distributed by Boyd Coffee Company, Portland, OR 97230***

Quantity: will be provided

Food: Spices & seasonings

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.

Part # - 1690. Lot # - 94675, 95467, 98145, 98764, 101858, 102489, 106319, 107267, 109189, 109281, 114634, and 116602.

Where it was sold

Washington

FDA's distribution note: Product distributed in Washington

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 soy; 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
Boyd Coffee Co
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 12, 2012
In FDA report of
Oct 10, 2012
Terminated
Nov 20, 2012
FDA recall number
F-0006-2013 · event 63177
Official record
FDA enforcement report search

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