Check the Batch
Class IITerminated in FDA datasetRecall initiated Feb 9, 2018

White Quinoa; 16 oz. (454g) bags with clear panel in front

Recalling firm: InHarvest, Inc.

Why it was recalled

Firm was notified by customer that some bags of White Quinoa actually contain Israeli Couscous and therefore do not declare wheat as an ingredient or allergen.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 23, 2018.

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Compare the exact product and package details with the label you have.

ProductWhite Quinoa; 16 oz. (454g) bags with clear panel in front; UPC: 0 72431 00195 6 Brand name Lunds & Byerlys Quinoa ingredients: White Quinoa Couscous ingredients: Israeli Couscous (wheat flour, rosemary extract). Contains: Wheat. Produced for Lunds & Byerlys, Edina, MN.
Package size16 oz
UPC072431001956

FDA code information

Best by Feb 11, 2019

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Full FDA record and distribution details

Original product description

White Quinoa; 16 oz. (454g) bags with clear panel in front; UPC: 0 72431 00195 6 Brand name Lunds & Byerlys Quinoa ingredients: White Quinoa Couscous ingredients: Israeli Couscous (wheat flour, rosemary extract). Contains: Wheat. Produced for Lunds & Byerlys, Edina, MN.

Extracted codes and context

TypeCode / valueContext
UPC072431001956White Quinoa; 16 oz. (454g) bags with clear panel in front; UPC: 0 72431 00195 6 Brand name Lunds & Byerlys Quinoa ingredients: White Quinoa Couscous ingredients: Israeli Couscous (wheat flou
best byFeb 11, 2019Best by Feb 11, 2019

Original FDA recall reason

Firm was notified by customer that some bags of White Quinoa actually contain Israeli Couscous and therefore do not declare wheat as an ingredient or allergen.

Recall details

Recall number
F-0830-2018
Event ID
79208
FDA status
Terminated
Initiated
Feb 9, 2018
Reported
Mar 7, 2018
Classified
Feb 23, 2018
Terminated
Feb 23, 2018
Quantity
120 cases (12 x 16 oz. bags per case)
Location
Woodland, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

One customer in MN

FDA source record · F-0830-2018

Data updated September 16, 2026. View official FDA data ↗

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