Spermidine — Class I food recall F-0729-2025
Terminated recall by Supplement Manufacturing Partner Inc., reported 2025-04-30, distributed nationwide. Undeclared allergen: Wheat
| Recall number | F-0729-2025 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Supplement Manufacturing Partner Inc., Largo, FL, United States |
| Recall initiated | 2025-04-04 |
| Classified | 2025-04-22 |
| Reported by FDA | 2025-04-30 |
| Terminated | 2025-09-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | DE |
| Quantity | 6,465 bottles |
| Reason classes | undeclared allergen |
| Allergens | wheat |
| Lot numbers | 12792402-44 |
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
Reason for recall
Undeclared allergen: Wheat
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0729-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.