FDA recall record

Woodstock Farms 7.5 OZ in a gusseted re-sealable poly bag recall — FDA F-0886-2013

Undeclared soy ingredient on mislabeled back panel. While the Tamari Almonds contain soy, the ingredient statement does not include soy. In addition, the…

Class Iclassification
F-0886-2013official record ID
Jan 23, 2013report date

Recall record at a glance

Official recordF-0886-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmWoodstock Farms
Report dateJan 23, 2013
Recall initiation dateJan 8, 2013
Quantity67 cases, each containing 8 packages per shipping case
LocationEdison, NJ, United States

Official product description

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

Why the product was recalled

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.

Distribution information

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

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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