NatureAll Heart-Plus Recall: Undeclared Soy Allergen
NatureAll recalls Heart-Plus dietary supplements due to undeclared soy. Check your bottle lot numbers for details on this Class II recall.
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Undeclared allergens: soy (lecithin)
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What happened, in plain English
NatureAll-STF Holding, LLC is recalling Heart-Plus, No. 83, a 120-capsule dietary supplement because it contains undeclared soy (lecithin). This poses a risk to individuals with soy allergies who may not be aware of the ingredient. The recall affects approximately 598 bottles distributed nationwide. Read more at govinfonow.com/recall/20629-natureall-heart-plus-recall-undeclared-soy-allergen.
Source Summary by GovInfoNow · govinfonow.com/recall/20629-natureall-heart-plus-recall-undeclared-soy-allergen · Updated October 11, 2026 · FDA enforcement record: FDA #F-3370-2017
Cite this page
“NatureAll Heart-Plus Recall: Undeclared Soy Allergen.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/20629-natureall-heart-plus-recall-undeclared-soy-allergen. Based on FDA recall #F-3370-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3370-2017%22&limit=1).
Why it’s dangerous
The supplement contains undeclared soy lecithin, which can trigger allergic reactions in people sensitive to soy. For those with severe allergies, accidental ingestion can lead to serious health consequences ranging from hives to anaphylaxis.
Who’s affected
Consumers who purchased Heart-Plus, No. 83 dietary supplements, particularly those with known soy allergies or sensitivities. Anyone in the listed states (CA, FL, GA, ID, IL, IN, TX, UT, WA, WY) who bought this product is potentially affected.
How to tell if you have this one
Check your bottle for the label 'Heart-Plus, No. 83, 120 Capsules, Dietary Supplement' manufactured by NatureAll-STF Holding, LLC. Specifically look for Lot numbers 40800915 or 44300217 on the packaging.
- Brand
NatureAll- Category
Food
All 8 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Status
Terminated- Distribution
Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
| Recall number | Product, codes & lots | Quantity | Class |
|---|---|---|---|
| F-3367-2017 | Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,; Lot 43200916, Exp 9/2019 | 367 bottles. | Class I |
| F-3368-2017 | Metabo-Plus, Garlic/Papaya Plus, No. 103, 90 Capsules, Dietary Supplement; Lot 39700615, Exp 6/2018 | 254 bottles. | Class I |
| F-3369-2017 | Thymus Plus, No. 114, 90 Capsules, Dietary Supplement; Lot 43701116, Exp 11/2019 | 107 bottles. | Class I |
| F-3370-2017 | Heart-Plus, No. 83, 120 Capsules, Dietary Supplement; Lot 40800915 & 44300217 | 598 bottles. | Class II |
| F-3371-2017 | Liver-Plus, No. 111 & 115, 120 Capsules, Dietary Supplement; Lot 43000816 & 45000417 | 400 bottles. | Class II |
| F-3372-2017 | Pancreas-Plus, No. 112, 90 Capsules, Dietary Supplement; Lot 42100516 & 45400517 | 566 bottles. | Class II |
| F-3373-2017 | Prostate-Plus, No. 117, 90 Capsules, Dietary Supplement; Lot 42700616 | 186 bottles. | Class II |
| F-3374-2017 | Leci-thin-Plus, No. 88, 90 Capsules, Dietary Supplement; Lot 41400116 | 80 bottles. | Class II |
What to do — step by step
Stop consuming the product
Do not take the capsules if you have them, especially if you are allergic to soy.
Check your lot numbers
Verify that your bottle matches Lot 40800915 or 44300217 to confirm it is part of this recall.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 10 states.
FDA distribution: “Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Florida, Georgia, Idaho, Illinois, Indiana, Texas, Utah, Washington, Wyoming.
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.
Questions people ask
Where was this product sold?
The product was distributed nationwide in the US, specifically in California, Florida, Georgia, Idaho, Illinois, Indiana, Texas, Utah, Washington, and Wyoming.
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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-3370-2017 (July 26, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3370-2017 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.