RecallRadar
FDA · FoodClass I

Jalux America Inc food recall: Drycapot cookie

Undeclared allergens

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
97242
Recall initiated
Jul 10, 2025
Classified by FDA
Jul 28, 2025
Posted in Enforcement Report
Aug 6, 2025
Terminated
Sep 9, 2025
Recalling firm
Jalux America Inc
Firm location
El Segundo, CA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Other
Products in this event
2

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

Undeclare Tree Nuts (almond, macadamia nut)

Undeclared Milk

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 Jul 10, 2025. FDA classified it 18 days later, on Jul 28, 2025. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: CA, IL, WA

Recalled products (2)

  • H-0347-2025 Class I Terminated

    Drycapot cookie, net weight: 1.15 oz UPC#: 4 942737 210191

    Codes / lots: Best Before date: September 26, 2025

    Quantity: 28 units

  • H-0348-2025 Class I Terminated

    Lespoir cookie, net weight: 1.41 oz. UPC# 4 942737 200147

    Codes / lots: Best Before date: September 26, 2025

    Quantity: 32 units

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 97242
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.