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FDA source record Class I Terminated

Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumption, shelf life: 24 months, PETE/White/150cc Plastic bottl...

Recall Date: 2025-04-04 Recalling Firm: Supplement Manufacturing Partner Inc. Record Ref: F-0729-2025

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumption, shelf life: 24 months, PETE/White/150cc Plastic bottl... and names Supplement Manufacturing Partner Inc. as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Supplement Manufacturing Partner Inc.
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2025-04-04
Best identifiers to check for a FDA record

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Product Description & Identification

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 / Hazard Identified

Undeclared allergen: Wheat

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Product was distributed throughout the United States and Germany.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0729-2025
Indexed update
2026-08-09 21:59:13 UTC
Official source
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