Seely Family Farm Spearmint Candy Canes Recall: Undeclared Soy Lecithin
Seely Family Farm recalls Spearmint candy canes (UPC 8 54502 00321 8) due to undeclared soy lecithin. Consumers should check product details and contact the company for guidance.
Lower-risk recall
Spearmint candy canes are recalled due to undeclared soy lecithin.
Contact the company
What happened, in plain English
Seely Family Farm is recalling Spearmint candy canes that contain undeclared soy lecithin. This means the product may not be safe for people with soy allergies, as the soy lecithin is a common allergen. Read more at govinfonow.com/recall/22875-seely-family-farm-spearmint-candy-canes-recall-undeclared-soy-lecithin.
Source Summary by GovInfoNow · govinfonow.com/recall/22875-seely-family-farm-spearmint-candy-canes-recall-undeclared-soy-lecithin · Updated October 8, 2026 · FDA enforcement record: FDA #F-0599-2017
Cite this page
“Seely Family Farm Spearmint Candy Canes Recall: Undeclared Soy Lecithin.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22875-seely-family-farm-spearmint-candy-canes-recall-undeclared-soy-lecithin. Based on FDA recall #F-0599-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0599-2017%22&limit=1).
Why it’s dangerous
Soy lecithin is a common allergen that can cause allergic reactions in sensitive individuals. The product was sold without clear labeling of this ingredient, which is a risk for people with soy allergies.
Who’s affected
People with soy allergies are at risk from these candy canes. The recall affects consumers who purchased the specific product with the UPC 8 54502 00321 8.
How to tell if you have this one
Check for the UPC 8 54502 00321 8 on the product packaging. The candy canes have a net weight of 1.4 ounces and were produced with lot code 11052016.
- Brand
Seely Family Farm- Product
Spearmint candy canes, Net wt. 1.4 oz. The UPC is 8 54502 00321 8- Category
Food
What to do — step by step
Check Product Details
Look for the UPC 8 54502 00321 8 on the packaging to confirm you have the recalled product.
Where it went and when
Where it was distributed
Distributed in Indiana and Washington.
FDA distribution: “in WA only” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Indiana, Washington.
Recall timeline
FDA terminated this recall 3 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-0599-2017 (November 15, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0599-2017 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.