← FDA ENFORCEMENT
F-0729-2025Class I

Supplement Manufacturing Partner Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Supplement Manufacturing Partner Inc.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-04-30
Distribution
Product was distributed throughout the United States and Germany.
Firm state
FL
Product quantity
6,465 bottles
Initiated by
Voluntary: Firm initiated
Reason for recall

Undeclared allergen: Wheat

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

Code / lot info

Lot 12792402-44

Other recalls SPEQ maps to Documentation & Change Control
See all Documentation & Change Control recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →