Streit's Quinoa with Mushrooms & Herbs Recall: Undeclared Sulfites Found
Streit's Quinoa with Mushrooms & Herbs (7.7 oz) from Israel contains undeclared sulfites at 57 ppm and 10 ppm. Consumers should check lot numbers 0045 and 2743 for affected products.
Lower-risk recall
The Commonwealth of Virginia sampled the product and revealed the presence of undeclared sulfites at 57 ppm and 10 ppm
Contact the company
What happened, in plain English
Streit's Quinoa with Mushrooms & Herbs (7.7 oz) from Israel has been recalled due to undeclared sulfites detected in samples from Virginia. This could pose a risk for people with sulfite allergies, though the product is not intended for consumption by those with severe allergies. Read more at govinfonow.com/recall/22854-streit-s-quinoa-with-mushrooms-herbs-recall-undeclared-sulfites-found.
Source Summary by GovInfoNow · govinfonow.com/recall/22854-streit-s-quinoa-with-mushrooms-herbs-recall-undeclared-sulfites-found · Updated October 8, 2026 · FDA enforcement record: FDA #F-0945-2017
Cite this page
“Streit's Quinoa with Mushrooms & Herbs Recall: Undeclared Sulfites Found.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22854-streit-s-quinoa-with-mushrooms-herbs-recall-undeclared-sulfites-found. Based on FDA recall #F-0945-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0945-2017%22&limit=1).
Why it’s dangerous
The product contains undeclared sulfites at levels of 57 ppm and 10 ppm, which can trigger allergic reactions in sensitive individuals. Sulfites are common food preservatives but can cause health issues in people with allergies.
Who’s affected
People with sulfite allergies may be affected by this product. Those who have consumed the recalled quinoa are at risk of allergic reactions.
How to tell if you have this one
Check for lot numbers 0045 and 2743 on the product label. The product is a 7.7 oz (220g) quinoa with mushrooms and herbs from Israel.
- Brand
Streit's- Category
Food
What to do — step by step
Check Product Lot Number
Look for lot numbers 0045 or 2743 on the product label.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “IL, MD, CA, & IL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Illinois, Maryland.
Recall timeline
FDA terminated this recall 19 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0945-2017 (November 18, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0945-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.