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Class I: serious health riskTerminated

Supplement Manufacturing Partner Spermidine Recall

Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplem…

Supplement Manufacturing Partner Inc. · Largo, FL

Risk level
Class I
Reported by FDA
Apr 30, 2025
Recall ID
F-0729-2025
Check your lot numberHow we source this data

Summary

Supplement Manufacturing Partner recalled Spermidine starting Apr 4, 2025. The FDA classified it as Class I (serious health risk) and published enforcement report F-0729-2025 on Apr 30, 2025. Reason: Undeclared allergen: Wheat. Status: Terminated.

Why it was recalled

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

Lot numbers, UPCs & expiration codes

Lot 12792402-44

Where it was sold

Product was distributed throughout the United States and Germany.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0729-2025
Classification
Class I
Status
Terminated
Recall initiated
Apr 4, 2025
FDA report date
Apr 30, 2025
Quantity
6,465 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Supplement Manufacturing Partner Inc.

Original FDA data

Every field from FDA enforcement report F-0729-2025, exactly as published.

Show all FDA fields
City
Largo
State
FL
Status
Terminated
Country
United States
Event ID
96657
Address
12333 Enterprise Blvd
Code information
Lot 12792402-44
Postal code
33773-2710
Report date
Apr 30, 2025
Product type
Food
Recall number
F-0729-2025
Classification
Class I
Recalling firm
Supplement Manufacturing Partner Inc.
Product quantity
6,465 bottles
Termination date
Sep 3, 2025
Reason for recall
Undeclared allergen: Wheat
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
Product was distributed throughout the United States and Germany.
Recall initiation date
Apr 4, 2025
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 22, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0729-2025, published Apr 30, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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