New Seasons Market Hot & Sour Broth Recall: Soy Not Listed on Label
New Seasons Market recalls 24 oz glass jar Hot & Sour Broth due to soybeans not being listed on label. This affects consumers with soy allergies.
Lower-risk recall
Hot & Sour Broth product contains Tamari which contains sub ingredient soybeans but finished label does not declare soy.
Contact the company
What happened, in plain English
New Seasons Market is recalling its 24 oz glass jar Hot & Sour Broth because the product contains soybeans but the label does not list soy. This poses a risk for people with soy allergies. Read more at govinfonow.com/recall/18243-new-seasons-market-hot-sour-broth-recall-soy-not-listed.
Source Summary by GovInfoNow · govinfonow.com/recall/18243-new-seasons-market-hot-sour-broth-recall-soy-not-listed · Updated October 5, 2026 · FDA enforcement record: FDA #F-0431-2019
Cite this page
“New Seasons Market Hot & Sour Broth Recall: Soy Not Listed on Label.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/18243-new-seasons-market-hot-sour-broth-recall-soy-not-listed. Based on FDA recall #F-0431-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0431-2019%22&limit=1).
Why it’s dangerous
The product contains soybeans but the label does not declare soy. This means individuals with soy allergies could be exposed to soy without knowing it, potentially causing allergic reactions.
Who’s affected
People with soy allergies are at risk from this product. The recall affects consumers who purchased the 24 oz glass jar Hot & Sour Broth from New Seasons Market.
How to tell if you have this one
Check for the 24 oz glass jar packaging with UPC 840600108672. The product is sold under New Seasons Market brand.
- Brand
New Seasons Market- Product
New Seasons Market Hot & Sour Broth, packaged in 24 oz glass jar. UPC 840600108672- Category
Food
What to do — step by step
Check Label for Soy
Look for soy listed on the label; if not present, the product is recalled.
Where it went and when
Where it was distributed
Distributed in Oregon and Washington.
FDA distribution: “distributed to retail stores in Oregon and Washington” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Oregon, Washington.
Recall timeline
FDA terminated this recall 4 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-0431-2019 (October 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0431-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.