Supplement Manufacturing Partner Inc. recalls 120-capsule Spermidine supplement due to undeclared wheat allergen. Consumers should check product details and contact for remedy.
Undeclared allergen: Wheat
Supplement Manufacturing Partner Inc. is recalling Spermidine Maximum Strength dietary supplements because they contain undeclared wheat, which can cause allergic reactions in sensitive individuals. This recall affects consumers who have wheat allergies or are at risk of allergic reactions.
The supplement contains undeclared wheat as an ingredient, which can trigger allergic reactions in individuals with wheat allergies. This is a food safety issue that requires immediate attention for those with allergies.
People who have wheat allergies or are sensitive to wheat may experience allergic reactions. The recall applies to consumers who purchased the supplement from any retailer.
Check for the product name 'Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules'. The product was sold in PETE/White/150cc Plastic bottles with a lot number starting with 12792402-44.
Look for the product name and lot number on the bottle to confirm if it's affected.
The recall is specifically for individuals with wheat allergies. People without allergies should not be at risk.
Check the product name and lot number on the bottle. The product name is 'Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules' and the lot number starts with 12792402-44.
The recall does not specify a remedy, so contact the manufacturer for further instructions.
We’ve drafted a message you can send Supplement Manufacturing Partner Inc. to request your refund or repair — edit it as you like.
Subject: Recall F-0729-2025 — Supplement Manufacturing Partner Inc. Supplement Manufacturing Partner Inc. Hello, I own a Supplement Manufacturing Partner Inc. that is covered by recall F-0729-2025 from Supplement Manufacturing Partner Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
