Agebox Recalls iKids-Growth Capsules Due to Undeclared Ibutamoren

FDA Recalls medium FDA · · United States

Agebox is voluntarily recalling 665 bottles of iKids-Growth (Day Formula) capsules because they contain undeclared ibutamoren and were marketed without FDA approval.

What Happened

Agebox has initiated a voluntary recall of its iKids-Growth (Day Formula) capsules. The recall was triggered because the product contains undeclared ibutamoren and is being marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). The FDA has classified this as a Class II recall.

Which Products Are Affected

The recall affects 665 bottles of Agebox iKids-Growth (Day Formula), 60-count bottles. The products are labeled as “Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA.”

Product Details:

  • UPC: 8 50065 59701 0
  • Lot # 23101201 (Expiration: 09/2026)
  • Lot # 24080801 (Expiration: 07/2027)
  • Lot # 25020701 (Expiration: 01/2028)

These products were distributed nationwide across the United States through Agebox.com (via Shopify) and Amazon.com. All orders were shipped directly to customers by Agebox.

What You Should Do

Consumers who have purchased the affected lots of iKids-Growth (Day Formula) should stop using the product immediately. For further information regarding returns or questions about the recall, consumers may contact Agebox at their Wilmington, Delaware headquarters. The firm initially notified customers of the recall via e-mail on October 28, 2025.

Why This Matters

The presence of undeclared pharmaceutical ingredients like ibutamoren in a dietary supplement poses potential health risks to consumers. Furthermore, marketing such products without required FDA approvals violates federal safety regulations designed to ensure drug efficacy and safety.

Source

FDA (Recall Number: D-0344-2026)

Source: FDA Official Notice

Frequently Asked Questions

What is this fda recalls alert about?
Agebox is voluntarily recalling 665 bottles of iKids-Growth (Day Formula) capsules because they contain undeclared ibutamoren and were marketed without FDA approval.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How severe is this alert?
This alert is classified as "medium" severity. Stay informed and follow agency guidance.
What area is affected?
This alert affects United States. Check with FDA for the most current geographic scope.
Where can I find more fda recalls alerts?
Browse all fda recalls alerts on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.