Drug recall
Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc…
FDA recall event 98011 · Class II · Agebox
Key facts
| Event ID | 98011 |
|---|---|
| Recall numbers | D-0344-2026, D-0345-2026 |
| Recalling firm | Agebox |
| Product type | Drugs |
| Products | Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 8 50065 59701 0, Agebox iKids-Growth (Night Formula), 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 850065597027 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren |
| Initiation date | Oct 28, 2025 |
| Report date | Mar 4, 2026 |
| City | Wilmington |
| State | DE |
| Country | United States |
| FEI number | 3038759360 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: