FDA recall record

Scenic Fruit Co Woodstock Frozen Organic Pomegranate Kernels are sold in 8 oz recall — FDA F-0702-2014

Woodstock Frozen Organic Pomegranate Kernels, 8 oz. pouches, are recalled based on epidemiological evidence that they may to be contaminated with…

Class Iclassification
F-0702-2014official record ID
Dec 11, 2013report date

Recall record at a glance

Official recordF-0702-2014
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmScenic Fruit Co
Report dateDec 11, 2013
Recall initiation dateJun 26, 2013
Quantity5,091 cases/12 bags/8 oz.
LocationGresham, OR, United States

Official product description

Woodstock Frozen Organic Pomegranate Kernels are sold in 8 oz. (227 gram) re-sealable plastic pouches with the UPC 0 42563 01628 9. The product is labeled in parts: "***WOODSTOCK***ORGANIC POMEGRANATE KERNELS***Juicy Lil' JEWELS***USDA ORGANIC***NET WT. 8 OZ (227g)***KEEP FROZEN***INGREDIENTS: Organic pomegranate kernels***Distributed by Woodstock, 313 Iron Horse Way Providence, RI 02908***".

Why the product was recalled

Woodstock Frozen Organic Pomegranate Kernels, 8 oz. pouches, are recalled based on epidemiological evidence that they may to be contaminated with hepatitis A.

Distribution information

Product was directly distributed to distribution centers in California, Colorado, Connecticut, Florida, Georgia, Indiana, Iowa, New Hampshire, Pennsylvania, Rhode Island, Texas, and Washington.

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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