FDA recall record

Global Juices & Fruits Nature's Earthly Choice Organic Lentil Trio product containing recall — FDA F-0878-2020

Gluten-Free lentils product tested positive for gluten and some pouches were found to contain barley, wheat, and possibly other gluten-containing grains.

Class IIclassification
F-0878-2020official record ID
Apr 15, 2020report date

Recall record at a glance

Official recordF-0878-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGlobal Juices & Fruits LLC
Report dateApr 15, 2020
Recall initiation dateMar 2, 2020
Quantity5070 cases or 30,420 pouches total
LocationEagle, ID, United States

Official product description

Nature's Earthly Choice Organic Lentil Trio product containing a blend of red split, black and green lentils, labeled Gluten-Free, packaged in stand up resealable pouch, 12 oz. (340 g), UPC 6 79948 10006 8. The product's label is read in parts: "*** Gluten-Free *** ORGANIC LENTIL TRIO ***Red Split, Green and Black Lentils *** INGREDIENTS: ORGANIC RED LENTILS, ORGANIC GREEN LENTILS, AND ORGANIC BLACK LENTILS*** LENTILS ARE FROM USA AND/OR CANADA*** Packed in the USA ***Distributed by: Natures's Earthly Choice Eagle, ID 83616***".

Why the product was recalled

Gluten-Free lentils product tested positive for gluten and some pouches were found to contain barley, wheat, and possibly other gluten-containing grains.

Distribution information

distributed in IL, NY, and OH.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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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