Food Recall Check
Class I · High risk Terminated Initiated Apr 4, 2025 (2 years ago)

Spermidine Maximum Strength recall

Recalled by Supplement Manufacturing Partner Inc. · Largo, FL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared allergen: Wheat

Undeclared allergen: Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Quantity: 6,465 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 12792402-44

Where it was sold

Nationwide.

FDA's distribution note: Product was distributed throughout the United States and Germany.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Supplement Manufacturing Partner Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 4, 2025
In FDA report of
Apr 30, 2025
Terminated
Sep 3, 2025
FDA recall number
F-0729-2025 · event 96657
Official record
FDA enforcement report search

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