CLASS II ONGOING Drug recall · Reported 4 Mar 2026 · FDA Enforcement Report
iKids-Growth (Day Formula) capsules recalled by Agebox
Agebox is recalling Agebox iKids-Growth (Day Formula) capsules, Manufactured Exclusively For: Agebox Inc, distributed nationwide in the US. The recall was initiated on 28 Oct 2025 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0344-2026
- FDA event ID
- 98011
- Recalling firm
- Agebox, Wilmington, DE
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 28 Oct 2025
- FDA classified
- 25 Feb 2026
- Reported
- 4 Mar 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Labeling Errors
Timeline
| 28 Oct 2025 | Recall initiated by company | |
| 25 Feb 2026 | Classified by FDA | +120 days |
| 4 Mar 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Product as listed by the FDA
Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 8 50065 59701 0
Where it was distributed
The product was distributed nationwide in the U.S. Agebox sells its U.S. products through Agebox.com (using Shopify) and Amazon.com. All orders are shipped to customers by Agebox itself; other parties are not involved in the distribution of the physical product.
Stores named: Amazon, Online Retailers
Questions about this recall
Is iKids-Growth (Day Formula) capsules, Manufactured Exclusively For: Agebox Inc recalled?
Yes. Agebox recalled iKids-Growth (Day Formula) capsules, Manufactured Exclusively For: Agebox Inc on 28 Oct 2025. The recall is Class II and its status is Ongoing. Recall number D-0344-2026.
Why was it recalled?
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Which lots are affected?
Lot # 23101201 exp 09/2026, 24080801 exp 07/2027, and 25020701 exp 01/2028
Where was it sold?
The product was distributed nationwide in the U.S. Agebox sells its U.S. products through Agebox.com (using Shopify) and Amazon.com. All orders are shipped to customers by Agebox itself; other parties are not involved in the distribution of the physical product.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Agebox
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | iKids-Growth (Night Formula), Manufactured Exclusively recalled | Agebox | Labeling Errors | Nationwide |