Food recall
Supplement Manufacturing Partner Inc. recall: Spermidine, Maximum Strength
Supplement Manufacturing Partner Inc., of Largo, FL, recalled Spermidine, Maximum Strength. The FDA's reason: “Undeclared allergen: Wheat.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on April 4, 2025, and the FDA first listed it in its Enforcement Report of April 30, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class I
It could cause serious harm or death
Why
Allergen not on the label
Status
Terminated
Closed September 3, 2025
The recall
- Company
- Supplement Manufacturing Partner Inc. (Largo, FL)
- Reason, in FDA's words
- “Undeclared allergen: Wheat”
- Where it was sold
- Product was distributed throughout the United States and Germany.
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 96657
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-0729-2025 Class I
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: Lot 12792402-44
Quantity: 6,465 bottles
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of April 30, 2025.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.