F-0729-2025
Supplement Manufacturing Partner Inc.
Data retrieved 2026-10-27T22:06:49.008Z
Site-assigned category (for this product recall): Allergen & mislabeling
Independent website; not affiliated with or endorsed by FDA. Recall information is attributed to the linked FDA record. Categories are assigned by this website using keyword rules; they are not FDA classifications or independent legal findings and may be incomplete or incorrect. A category summarizes the stated reason for the identified product recall, not a finding about the firm generally or its other products. FDA’s original reason text appears below.
Official openFDA record · FDA recalls and safety alerts
Fields as reported by FDA
Dates are formatted YYYY-MM-DD. “Not reported” means the field was absent or empty.
- recall_number
- F-0729-2025
- event_id
- 96657
- recalling_firm
- Supplement Manufacturing Partner Inc.
- city
- Largo
- state
- FL
- country
- United States
- 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
- classification
- Class I
- FDA-reported status (not current status)
- Terminated
FDA does not update this status after recall classification. It may not reflect whether the recall is currently ongoing, completed, or terminated. - voluntary_mandated
- Voluntary: Firm initiated
- distribution_pattern
- Product was distributed throughout the United States and Germany.
- product_quantity
- 6,465 bottles
- code_info
- Lot 12792402-44
- recall_initiation_date
- 2025-04-04
- report_date
- 2025-04-30
- termination_date
- 2025-09-03