Heart-Plus, No. 83, 120 Capsules, Dietary Supplement

Undeclared allergens: soy (lecithin)

Recall #: F-3370-2017
Affected scope: 598 bottles.
Initiated: July 26, 2017

Compiled from official public sources by the publisher. · Updated September 2026

NatureAll-STF Holding, LLC recalled Heart-Plus, No. 83, 120 Capsules, Dietary Supplement - a moderate-severity action.

Heart-Plus, No. 83, 120 Capsules, Dietary Supplement was recalled by NatureAll-STF Holding, LLC in August 23, 2017. Reason: Undeclared allergens: soy (lecithin). Check the official notice for the remedy. Verify recall #F-3370-2017 with the FDA Food before acting.

The recall

NatureAll-STF Holding, LLC issued this moderate-severity FDA Food recall-Undeclared allergens: soy (lecithin).

Moderate
severity level: Class II
classification: August 23, 2017
reported

Sourced from official FDA Food enforcement records. Verify recall #F-3370-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 5 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Heart-Plus, No. 83, 120 Capsules, Dietary Supplement

Reason for recall

Undeclared allergens: soy (lecithin)

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	F-3370-2017
Date reported	August 23, 2017
Date initiated	July 26, 2017
Recalling firm	NatureAll-STF Holding, LLC
Firm location	Salt Lake City, UT
Affected scope	598 bottles.
Distribution	Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-3370-2017) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Heart-Plus, No. 83, 120 Capsules, Dietary Supplement. Recalled by NatureAll-STF Holding, LLC. Units affected: 598 bottles..

Why was this product recalled? ▼

Undeclared allergens: soy (lecithin)

Which agency issued this recall? ▼

This recall was issued by the FDA Food on August 23, 2017. Severity: Moderate. Recall number: F-3370-2017.

Where was the recalled product distributed? ▼

Distribution: Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees..

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Moderate), closest by report date among other firms and states.

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Similar Dietary Supplements · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

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This recall: FDA Food, reported August 23, 2017. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026