HIGH

Agebox iKids-Growth Capsules Recalled Over Undeclared Ingredient

AGEBOX Inc. recalled 665 bottles of iKids-Growth capsules on October 28, 2025, due to undeclared ibutamoren. The product was marketed without an approved NDA/ANDA. Consumers should stop using the product immediately and contact Agebox for guidance.

Quick Facts at a Glance

Recall Date
October 28, 2025
Hazard Level
HIGH
Brand
Agebox
Category
Health & Personal Care
Sold At
Amazon, Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

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

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Agebox or your healthcare provider for guidance. Notification method: E-Mail

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Product Details

The recall involves Agebox iKids-Growth (Day Formula) capsules in 60-count bottles. The affected lot numbers are 23101201 exp 09/2026, 24080801 exp 07/2027, and 25020701 exp 01/2028. The product was sold through Agebox.com and Amazon.

The Hazard

The product contains undeclared ibutamoren, a substance that may pose health risks. This recall is classified as Class II, indicating a potential for serious health consequences.

Reported Incidents

There have been no reported incidents or injuries associated with this recall at this time. Consumers are urged to be cautious regarding the undeclared ingredient.

What to Do

Stop using the product immediately. Contact Agebox or your healthcare provider for further guidance. Refunds are available by reaching out via email.

Contact Information

For more information, consumers can visit the Agebox website or contact the company via email. Additional details are available on the FDA's recall page.

Key Facts

  • Recall Date: October 28, 2025
  • Quantity Recalled: 665 bottles
  • Hazard: Undeclared ibutamoren
  • Class II Recall
  • Available for purchase on Agebox.com and Amazon

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Brand
Model Numbers
Lot # 23101201 exp 09/2026
24080801 exp 07/2027
and 25020701 exp 01/2028
Affected States
ALL
Report Date
March 4, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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