Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported April 30, 2025
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
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 FDA Food action (record #F-0729-2025) was formally reported on April 30, 2025, with the manufacturer initiating the action on April 4, 2025. It is classified under Critical severity (Class I), with a current status of Terminated. Supplement Manufacturing Partner Inc. is listed as the recalling firm, operating out of Largo, FL. Federal records list the affected scope as 6,465 bottles.
The documented reason for this recall is: Undeclared allergen: Wheat Distribution data in the federal record shows the product reached: Product was distributed throughout the United States and Germany.. Distribution scope 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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.
Affected scope
6,465 bottles
Related Recalls
6
0 from same agency
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
| 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? ▼
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. Recalled by Supplement Manufacturing Partner Inc.. Units affected: 6,465 bottles.
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..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0729-2025) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
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.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported April 30, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.