FDA Drug Recalls

Recalls / Class II

Class IID-0344-2026

Product

Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 8 50065 59701 0

Affected lot / code info
Lot # 23101201 exp 09/2026, 24080801 exp 07/2027, and 25020701 exp 01/2028

Why it was recalled

Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

Recalling firm

Firm
Agebox
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
108 W 13th St, N/A, Wilmington, Delaware 19801-1145

Distribution

Quantity
665 bottles
Distribution pattern
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.

Timeline

Recall initiated
2025-10-28
FDA classified
2026-02-25
Posted by FDA
2026-03-04
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0344-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls