Agebox recalls iKids-Growth Day Formula capsules due to undeclared ibutamoren. Check your 60-count bottles with specific lot numbers for affected items.
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Agebox is recalling iKids-Growth Day Formula capsules because they contain undeclared ibutamoren, a substance that requires FDA approval. This could pose health risks if taken without proper oversight.
The capsules contain ibutamoren, which is not approved by the FDA and was marketed without proper regulatory clearance. This could lead to health issues if consumed without medical supervision.
Parents or caregivers of children using Agebox iKids-Growth capsules. Children who have taken the capsules without knowing the undeclared ingredient are at risk.
Check for 60-count bottles with lot numbers 23101201 (expires 09/2026), 24080801 (expires 07/2027), or 25020701 (expires 01/2028).
Look for lot numbers 23101201, 24080801, or 25020701 on the 60-count bottles.
The capsules contain undeclared ibutamoren, which requires FDA approval but was marketed without it.
The recall record does not specify a remedy, so contact Agebox directly for guidance.
The recall indicates a potential health risk due to undeclared ibutamoren, but specific risks are not detailed in the record.
We’ve drafted a message you can send Agebox to request your refund or repair — edit it as you like.
Subject: Recall D-0344-2026 — Agebox Agebox Hello, I own a Agebox that is covered by recall D-0344-2026 from Agebox. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
