The Recall Desk
SevereFDA (Drugs)·D-0344-2026·Announced 2026-03-04

Agebox iKids-Growth Day Formula Capsules Recalled Over Undeclared Drug Ingredient

Agebox is recalling 665 bottles of iKids-Growth Day Formula capsules because they contain undeclared ibutamoren, a drug ingredient not approved for marketing in the U.S.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: This is an FDA Class II recall involving a product marketed without an approved NDA/ANDA due to the presence of undeclared ibutamoren, a pharmacologically active compound. Per the rubric, FDA Class II recalls with risk-of-harm characteristics where injury has not yet been reported are scored as Severe (4).

Plain-English summary

Agebox Inc. is recalling 665 bottles of Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, UPC 8 50065 59701 0. The recalled product includes lot numbers 23101201 exp 09/2026, 24080801 exp 07/2027, and 25020701 exp 01/2028.

The recall is being issued because the product contains undeclared ibutamoren, which is a drug ingredient that has not been approved by the FDA through a New Drug Application (NDA) or an Abbreviated New Drug Application (ANDA). Marketing a drug without an approved NDA/ANDA is a violation of the Federal Food, Drug, and Cosmetic Act.

The product was distributed nationwide in the U.S. through Agebox.com (using Shopify) and Amazon.com. All orders were shipped directly to customers by Agebox; no other parties were involved in the distribution of the physical product.

Consumers who have purchased Agebox iKids-Growth Day Formula capsules should stop using the product immediately and contact Agebox Inc. for a full refund. Consumers with questions can contact the company directly.

The recalled product

Product
Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 8 50065 59701 0
Manufacturer
Agebox
Category
Drug — Dietary Supplement / Undeclared Drug Ingredient
Hazard
Affected units
665

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Lot # 23101201 exp 09/2026
  • 24080801 exp 07/2027
  • and 25020701 exp 01/2028

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 2 recalled by Agebox under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Related recalls

Same manufacturer · Agebox

See all →

Same hazard · undeclared drug ingredient

See all →