Supplement Manufacturing Partner Inc. food recall: Spermidine
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 96657
- Recall initiated
- Apr 4, 2025
- Classified by FDA
- Apr 22, 2025
- Posted in Enforcement Report
- Apr 30, 2025
- Terminated
- Sep 3, 2025
- Recalling firm
- Supplement Manufacturing Partner Inc.
- Firm location
- Largo, FL, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Undeclared allergen: Wheat
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Apr 4, 2025. FDA classified it 18 days later, on Apr 22, 2025. Distribution reported by FDA: Product was distributed throughout the United States and Germany. Supplement Manufacturing Partner Inc. has 2 recalls in our records.
Recalled products (1)
F-0729-2025 Class I Terminated
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
Codes / lots: Lot 12792402-44
Quantity: 6,465 bottles
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 96657
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.