RecallRadar
FDA · FoodClass I

Art Monkey LLC dba Why Not Natural food recall: Why Not Natural Moringa Capsules 120 capsule bottle marked with lot #…

SalmonellaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
98367
Recall initiated
Jan 28, 2026
Classified by FDA
Feb 13, 2026
Posted in Enforcement Report
Feb 25, 2026
Terminated
Apr 3, 2026
Recalling firm
Art Monkey LLC dba Why Not Natural
Firm location
Houston, TX, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Potential to be contaminated with Salmonella

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Jan 28, 2026. FDA classified it 16 days later, on Feb 13, 2026. Distribution reported by FDA: Nationwide

Recalled products (1)

  • H-0510-2026 Class I Terminated

    Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom.

    Codes / lots: lot # A25G051

    Quantity: 8,500 bottles

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 98367
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.