RecallHawk
Class I Recall

Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumpti

Supplement Manufacturing Partner Inc.

Summary

The FDA issued a Class I for Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary by Supplement Manufacturing Partner Inc.. Reason: Undeclared allergen: Wheat.

Details

Source

Food Recall

External ID

F-0729-2025

Action Date

2025-04-30

Status

Terminated

Category

food

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/Code Info: Lot 12792402-44

Quantity Affected: 6,465 bottles

Reason for Recall

Undeclared allergen: Wheat

Distribution

Product was distributed throughout the United States and Germany.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-04-04

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 35 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Supplement Manufacturing Partner Inc. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Supplement Manufacturing Partner Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Supplement Manufacturing Partner Inc. have FDA actions?

Supplement Manufacturing Partner Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0729-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions