FDA recall record

It Takes A Village Foods Kale Crisps Zen Nori product is seaweed flavored dehydrated recall — FDA F-3048-2015

Kale Crisps Zen Nori is recalled due to undeclared SOY. Soybean is a sub-ingredient of the ingredient "Tamari" and soy is not declared on label.

Class Iclassification
F-3048-2015official record ID
Sep 2, 2015report date

Recall record at a glance

Official recordF-3048-2015
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmIt Takes A Village Foods, LLC
Report dateSep 2, 2015
Recall initiation dateJul 17, 2015
Quantity752 packages (1.5 oz. per package)
LocationHailey, ID, United States

Official product description

Kale Crisps Zen Nori product is seaweed flavored dehydrated kale chip, sold under brand Veggie Evolution, each poly pouch has a net weight 1.5 oz. There are six packages per case. UPC is 7 13757 57480 8. The product's label is read in part: "***VEGGIE EVOLUTION***KALE CRISPS***ZEN NORI***NET WT 1.5 OZ (43g)***INGREDIENTS: KALE, LEMON JUICE, UNREFINED TOASTED SESAME OIL, TAMARI, SESAME SEEDS, ONION, APPLE JUICE, GARLIC,WAKAME SEAWEED, RAISINS***ALLERGEN STATEMENT: MADE IN A FACILITY THAT USES DAIRY PRODUCTS***".

Why the product was recalled

Kale Crisps Zen Nori is recalled due to undeclared SOY. Soybean is a sub-ingredient of the ingredient "Tamari" and soy is not declared on label.

Distribution information

Distributed in Arkansas, Arizona, California, Colorado, Florida, Idaho, Kansas, Michigan, Montana, Nebraska, New Jersey, New Mexico, Oklahoma, Oregon, Pennsylvania, Texas, Utah, Washington and Wyoming. The firm also sold directly to internet consumers on line at VeggieEvolution.com. Internet consignees are located in CA, ID, MN, MS, OR, TX, UT, VA, and WA.

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: Press Release.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.