Teasource Roasted Chestnut Tea Recall: Undeclared Almonds in Loose Leaf Tea
Teasource recalls loose leaf Roasted Chestnut tea due to undeclared slivered almonds. Consumers should check product packaging for 16oz, 4oz, or 2oz bags sold in the US.
Lower-risk recall
Roasted Chestnut loose leaf tea contains undeclared slivered almonds.
Contact the company
What happened, in plain English
Teasource is recalling loose leaf Roasted Chestnut tea because it contains undeclared slivered almonds. This could pose a risk for people with nut allergies who might not be aware of the almonds in their tea. Read more at govinfonow.com/recall/18803-teasource-roasted-chestnut-tea-recall-undeclared-almonds-in-loose-leaf.
Source Summary by GovInfoNow · govinfonow.com/recall/18803-teasource-roasted-chestnut-tea-recall-undeclared-almonds-in-loose-leaf · Updated October 6, 2026 · FDA enforcement record: FDA #F-1841-2018
Cite this page
“Teasource Roasted Chestnut Tea Recall: Undeclared Almonds in Loose Leaf Tea.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18803-teasource-roasted-chestnut-tea-recall-undeclared-almonds-in-loose-leaf. Based on FDA recall #F-1841-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1841-2018%22&limit=1).
Why it’s dangerous
The tea contains slivered almonds that were not declared on the label. This could cause allergic reactions in people who are sensitive to nuts, especially if they are unaware the tea contains almonds.
Who’s affected
People who have purchased Teasource Roasted Chestnut loose leaf tea in 16oz, 4oz, or 2oz bags sold in the US are affected. Those with nut allergies are at higher risk due to the undeclared almonds.
How to tell if you have this one
Check for Teasource Roasted Chestnut loose leaf tea in 16oz (454g) metal/poly bags, 4oz, or 2oz resealable foil bags sold in the US. The product was distributed through teasource.com and physical stores in Roseville, MN.
- Brand
Teasource- Category
Food
What to do — step by step
Check Product Packaging
Look for the product name and packaging details on the tea bag to confirm it matches the recalled items.
Where it went and when
Where it was distributed
Distributed in 17 states.
FDA distribution: “AL, CO, FL, IA, ID, IL, IN, MI, MN, NC, ND, NY, OK, OR, SC, TX, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Colorado, Florida, Idaho, Illinois, Indiana, Iowa, Michigan, Minnesota, New York, North Carolina, North Dakota, Oklahoma, Oregon, South Carolina, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 47 days 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-1841-2018 (July 27, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1841-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.