HIGH

Agebox iKids-Growth Recalled Over Undeclared Ibutamoren

Agebox recalled its iKids-Growth Night Formula due to the presence of undeclared ibutamoren. The recall affects 60-count bottles manufactured exclusively for AGEBOX Inc. Consumers should stop using the product immediately and contact Agebox or their healthcare provider 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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

The recalled product is Agebox iKids-Growth (Night Formula), 60-count bottles. The affected lot numbers include 23101202 exp 09/2026, 24080802 exp 07/2027, and 25020702 exp 01/2028. The product was sold nationwide through Agebox.com and Amazon.

The Hazard

The product contains undeclared ibutamoren, a substance not approved for use in dietary supplements. The U.S. FDA classified this recall as Class II, indicating a potential risk of serious health issues.

Reported Incidents

There have been no reported injuries or incidents associated with this product recall. However, the presence of undeclared ibutamoren poses significant health risks.

What to Do

Stop using the Agebox iKids-Growth immediately. Contact Agebox or your healthcare provider for further guidance and to discuss potential health effects.

Contact Information

For more information, consumers can visit the Agebox website or contact them via email. For additional guidance, reach out to the FDA.

Key Facts

  • Recalled product: Agebox iKids-Growth (Night Formula)
  • Contains undeclared ibutamoren
  • Class II recall due to health risks
  • Stop using immediately and consult healthcare provider
  • Available through Agebox.com and Amazon

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

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

Product Details

Brand
Model Numbers
Lot # 23101202 exp 09/2026
24080802 exp 07/2027
and 25020702 exp 01/2028
Affected States
ALL
Report Date
March 4, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

Related Recalls

HIGH

AvKARE Recalls Amantadine HCl Capsules Over Dissolution Issues

AvKARE recalled Amantadine HCl capsules on February 13, 2026, due to failed dissolution specifications. The recall affects the 100 mg capsules, which may not dissolve properly. Consumers should stop using this product and contact their healthcare provider immediately.

AMANTADINE HCL
Failed Dissolution
Read more
HIGH

Eptifibatide Injection Recalled Over Labeling Error

Slate Run Pharmaceuticals recalled Eptifibatide Injection on February 12, 2026. The recall affects all lots of the 75 mg/100 mL vial due to incorrect dosing information. Healthcare providers and consumers must stop using the product immediately.

EPTIFIBATIDE
Labeling: Not
Read more
HIGH

LEO Pharma Recalls Adbry Injection Over Sterility Concerns

LEO Pharma Inc. recalled 11,407 units of Adbry injection on February 10, 2026. The recall stems from a lack of assurance of sterility due to particulate matter identified as wool fiber. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

ADBRY
Lack of
Read more
HIGH

Hitachi Proton Beam Therapy Device Recalled for Software Issues

Hitachi Ltd. recalled one unit of its Proton Beam Therapy System on February 6, 2026 due to a software anomaly. The issue may result in positional discrepancies during patient treatment. The recall affects distribution in Texas and Washington D.C.

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Software anomaly
Read more
HIGH

Hitachi Proton Beam Therapy System Recalled Due to Software Issue

Hitachi recalled its Proton Beam Therapy System on February 6, 2026, due to a software anomaly that may result in positional discrepancies. The recall affects one unit distributed in Texas and Washington D.C. Healthcare providers and patients must stop using the device immediately.

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Software anomaly
Read more
HIGH

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Fresenius Kabi Compounding recalled its vancomycin HCl injection on February 5, 2026, due to a lack of assurance of sterility. This Class II recall affects all lots distributed nationwide. Healthcare providers and consumers must stop using the product immediately.

Fresenius Kabi Compounding
Lack of
Read more