CLASS II Food recall · Reported 7 Mar 2018 · FDA Enforcement Report
White Quinoa recalled by InHarvest
InHarvest is recalling White Quinoa, distributed in Minnesota. The recall was initiated on 9 Feb 2018 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0830-2018
- FDA event ID
- 79208
- Recalling firm
- InHarvest, Woodland, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 9 Feb 2018
- FDA classified
- 23 Feb 2018
- Reported
- 7 Mar 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Wheat & Gluten
- Product category
- Flour
Timeline
| 9 Feb 2018 | Recall initiated by company | |
| 23 Feb 2018 | Classified by FDA | +14 days |
| 7 Mar 2018 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
Product as listed by the FDA
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.
Where it was distributed
One customer in MN
Questions about this recall
Why was it 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.
Which lots are affected?
Best by Feb 11, 2019
Where was it sold?
One customer in MN
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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