CLASS I Food recall · Reported 30 Apr 2025 · FDA Enforcement Report

Spermidine, Maximum Strength, 10 mg per serving recalled

Supplement Manufacturing Partner is recalling Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary, distributed nationwide in the US. The recall was initiated on 4 Apr 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 12792402-44
Quantity recalled6,465 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0729-2025
FDA event ID
96657
Recalling firm
Supplement Manufacturing Partner, Largo, FL
Classification
Class I
Status
Terminated
Recall initiated
4 Apr 2025
FDA classified
22 Apr 2025
Reported
30 Apr 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Allergens
Product category
Flour

Timeline

4 Apr 2025Recall initiated by company
22 Apr 2025Classified by FDA+18 days
30 Apr 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared allergen: Wheat

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

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

Where it was distributed

Product was distributed throughout the United States and Germany.

Nationwide

Questions about this recall

Why was it recalled?

Undeclared allergen: Wheat

Which lots are affected?

Lot 12792402-44

Where was it sold?

Product was distributed throughout the United States and Germany.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Supplement Manufacturing Partner

All 2
ReportedClassRecallCompanyReasonWhere
FoodCLASS IIHavasu Beetroot Powder recalled by Supplement ManufacturingHavasu BeetrootSupplement Manufacturing PartnerUndeclared MilkNationwide

Other Flour recalls

All 658