Capsules Recall: Agebox iKids-Growth (Night Formula)
Announced 2026-03-04 · FDA
FDA is recalling 665 bottles of Agebox iKids-Growth (Night Formula) capsules distributed nationwide in the United States due to marketing the product without an approved NDA/ANDA and the presence of undeclared ibutamoren. Lot numbers affected are 23101201 exp 09/2026, 24080801 exp 07/2027, and 25020701 exp 01/2028. Corrective actions have not been specified.
| Brand | Agebox |
|---|---|
| Product | Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 8 50065 59701 0 |
| Reason | Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren |
| Severity | moderate |
| Units affected | 665 bottles |
| Distribution | 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. |
| Agency | FDA |
| Recall / campaign no. | Lot # 23101201 exp 09/2026, 24080801 exp 07/2027, and 25020701 exp 01/2028 |
WHAT YOU SHOULD DO
- Stop using any capsules from the affected lots immediately.
- Check your bottle for Lot numbers 23101201, 24080801, or 25020701; if matching, dispose per local guidelines or follow Agebox disposal/return instructions on their website.
- If you have questions, contact Agebox via Agebox.com or the Amazon listing for guidance.
- If you have experienced adverse effects, seek medical advice and report them to the FDA MedWatch program.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.