CLASS II ONGOING Drug recall · Reported 4 Mar 2026 · FDA Enforcement Report

iKids-Growth (Night Formula), Manufactured Exclusively recalled

Agebox is recalling iKids-Growth (Night Formula), Manufactured Exclusively For: Agebox Inc., Wilmington, DE, 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

Lot, batch or date codesLot # 23101202 exp 09/2026, 24080802 exp 07/2027, and 25020702 exp 01/2028
Quantity recalledN/A

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-0345-2026
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
E-Mail
Reason category
Labeling Errors

Timeline

28 Oct 2025Recall initiated by company
25 Feb 2026Classified by FDA+120 days
4 Mar 2026Published 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 (Night Formula), 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 850065597027

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.

Nationwide

Stores named: Amazon, Online Retailers

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot # 23101202 exp 09/2026, 24080802 exp 07/2027, and 25020702 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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 98011
ReportedClassRecallCompanyReasonWhere
CLASS IIiKids-Growth (Day Formula) capsules recalled by AgeboxAgeboxLabeling ErrorsNationwide

More recalls from Agebox

All 2
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIiKids-Growth (Day Formula) capsules recalled by AgeboxAgeboxLabeling ErrorsNationwide