Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumption, shelf life: 24 months, PETE/White/150cc Plastic bottle/lid, 120 count.Supplement Facts: Spermidine 3HCL 10mg*** Other Ingredients: Hydroxypropyl Methylcellulose, Rice Flour

Undeclared allergen: Wheat

Recall #: F-0729-2025
Affected scope: 6,465 bottles
Initiated: April 4, 2025

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

Supplement Manufacturing Partner Inc. recalled Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplemen… - a critical-severity action.

Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplemen… was recalled by Supplement Manufacturing Partner Inc. in April 30, 2025. Reason: Undeclared allergen: Wheat. Check the official notice for the remedy. Verify recall #F-0729-2025 with the FDA Food before acting.

The recall

Supplement Manufacturing Partner Inc. issued this critical-severity FDA Food recall-Undeclared allergen: Wheat.

Critical
severity level: Class I
classification: April 30, 2025
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0729-2025 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 - 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 high severity.

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

Product description

Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumption, shelf life: 24 months, PETE/White/150cc Plastic bottle/lid, 120 count.Supplement Facts: Spermidine 3HCL 10mg*** Other Ingredients: Hydroxypropyl Methylcellulose, Rice Flour

Reason for recall

Undeclared allergen: Wheat

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Critical (Class I)
Status	Terminated
Recall number	F-0729-2025
Date reported	April 30, 2025
Date initiated	April 4, 2025
Recalling firm	Supplement Manufacturing Partner Inc.
Firm location	Largo, FL
Affected scope	6,465 bottles
Distribution	Product was distributed throughout the United States and Germany.

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-0729-2025) 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.
This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. 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? ▼

Why was this product recalled? ▼

Undeclared allergen: Wheat

Which agency issued this recall? ▼

This recall was issued by the FDA Food on April 30, 2025. Severity: Critical. Recall number: F-0729-2025.

Where was the recalled product distributed? ▼

Distribution: Product was distributed throughout the United States and Germany..

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 (Critical), closest by report date among other firms and states.

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This recall: FDA Food, reported April 30, 2025. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026