FDA recall, , Moderate risk
Agebox iKids-Growth Day and Night Formula Capsules
Agebox iKids-Growth (Day Formula) capsules contain undeclared ibutamoren.
Summary by Recall Canary from the FDA notice
What happened
Agebox of Wilmington, Delaware is recalling iKids-Growth (Night Formula) and iKids-Growth (Day Formula) capsules because they contain undeclared ibutamoren and were marketed without an approved NDA/ANDA. The recall began on October 28, 2025, and the products were distributed nationwide in the United States through Agebox.com and Amazon.com.
2 photos
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is your bottle affected?
2 products
Match the list below, then check the codes the FDA notice also names.
A UPC is the number printed under a barcode.
Agebox iKids-Growth (Day Formula) capsules, 60-count bottles
- UPC
- 23101201
- 24080801
- 25020701
Agebox iKids-Growth (Night Formula), 60-count bottles
- UPC
- 23101202
- 24080802
- 25020702
From the FDA notice
Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 8 50065 59701 0
Recall details
- Company began the recall
- Sold in
The product was distributed nationwide in the U.S. Agebox sells its U.S. products through Agebox.com (using Shopify) and Amazon.com. All orders are shipped to customers by Agebox itself; other parties are not involved in the distribution of the physical product.
- Company
- AgeboxWilmington, Delaware
- Hazard
- Hidden drug ingredient
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98011
- Recall numbers
- D-0344-2026 to D-0345-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
