Grandma's Herbs Cholesterol Support Supplement Recall: Undeclared Soy Lecithin
Grandma's Herbs recalls 100-capsule cholesterol support supplements due to undeclared soy lecithin. Consumers should check product details and contact the company for guidance.
Lower-risk recall
Grandma s Herbs Cholesterol has undeclared soy lecithin.
Contact the company
What happened, in plain English
Grandma's Herbs is recalling its 'Because They Work' cholesterol support supplements because they contain undeclared soy lecithin. This could affect people who have soy allergies or dietary restrictions. Read more at govinfonow.com/recall/20656-grandma-s-herbs-cholesterol-support-supplement-recall-undeclared-soy-lecithin.
Source Summary by GovInfoNow · govinfonow.com/recall/20656-grandma-s-herbs-cholesterol-support-supplement-recall-undeclared-soy-lecithin · Updated October 7, 2026 · FDA enforcement record: FDA #F-3409-2017
Cite this page
“Grandma's Herbs Cholesterol Support Supplement Recall: Undeclared Soy Lecithin.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20656-grandma-s-herbs-cholesterol-support-supplement-recall-undeclared-soy-lecithin. Based on FDA recall #F-3409-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3409-2017%22&limit=1).
Why it’s dangerous
The supplement contains undeclared soy lecithin, which is a soy-based ingredient. This poses a risk for individuals with soy allergies or who have dietary restrictions that require clear labeling.
Who’s affected
People who own or use the recalled cholesterol supplements are likely affected. Those with soy allergies or specific dietary needs are at higher risk.
How to tell if you have this one
Check for the product name 'Because They Work' GRANDMA'S HERBS CHOLESTEROL SUPPORT, 100 capsules, 480 mg, packaged in PET plastic bottles. The UPC number is 714938 00046 and lot number 13112.
- Brand
Grandma's Herbs- Product
"Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Dietary Supplement, 100 Capsules 480 mg. Packaging: PET- Category
Food
What to do — step by step
Check Product Details
Look for the product name, UPC number 714938 00046, and lot number 13112 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide. No foreign/military/govt accounts.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- 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-3409-2017 (July 20, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3409-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.