CLASS I Food recall · Reported 23 Jan 2013 · FDA Enforcement Report

Woodstock All Natural Tamari Almonds in a gusseted re-sealable recalled

Woodstock Farms is recalling Woodstock All Natural Tamari Almonds in a gusseted re-sealable, distributed in 26 states. The recall was initiated on 8 Jan 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest By: 10/24/13 Lot: 12298 UPC# 0-42563-00838-3

Quantity recalled67 cases, each containing 8 packages per shipping case

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0886-2013
FDA event ID: 64046
Recalling firm: Woodstock Farms, Edison, NJ
Brand: Woodstock
Classification: Class I
Status: Terminated
Recall initiated: 8 Jan 2013
FDA classified: 16 Jan 2013
Reported: 23 Jan 2013
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Undeclared Soy
Product category: Nuts

Timeline

8 Jan 2013	Recall initiated by company
16 Jan 2013	Classified by FDA	+8 days
23 Jan 2013	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared soy ingredient on mislabeled back panel. While the Tamari Almonds contain soy, the ingredient statement does not include soy. In addition, the nutrition facts and UPC# are incorrect which corresponds to another almond product. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume this product.

Product as listed by the FDA

Woodstock All Natural Tamari Almonds, 7.5 OZ in a gusseted re-sealable poly bag.

Where it was distributed

Alabama, Connecticut, Florida, Georgia, Illinois, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Vermont, Virginia, Wisconsin, and District of Columbia

Alabama Connecticut District of Columbia Florida Georgia Illinois Massachusetts Maryland Maine Michigan Minnesota Missouri North Carolina New Hampshire New Jersey New York Ohio Oklahoma Pennsylvania Rhode Island

Questions about this recall

Why was it recalled?

Which lots are affected?

Best By: 10/24/13 Lot: 12298 UPC# 0-42563-00838-3

Where was it sold?

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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