Class ITerminatedVoluntary: Firm initiated
Supplement Manufacturing Partner Inc.: food recall F-0729-2025
Supplement Manufacturing Partner Inc. of Largo, FL recalled Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral… Reason: Undeclared allergen: Wheat. The FDA listed it as Class I in its Enforcement Report dated Apr 30, 2025; distribution: nationwide.
Record status as published: Terminated (terminated Sep 3, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 6,465 bottles
- Reason for recall
- Undeclared allergen: Wheat
- Codes, lots and dates on the package
- Lot 12792402-44
- Distribution pattern
- Product was distributed throughout the United States and Germany.
- Recalling firm
- Supplement Manufacturing Partner Inc., Largo, FL
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Apr 4, 2025 |
| Classified by the FDA | Apr 22, 2025 |
| Published in the Enforcement Report | Apr 30, 2025 |
| Terminated | Sep 3, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0729-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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