CLASS I Food recall · Reported 6 Aug 2025 · FDA Enforcement Report

Lespoir cookie recalled by Jalux America

Jalux America is recalling Lespoir cookie, distributed in California, Illinois, Washington. The recall was initiated on 10 Jul 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest Before date: September 26, 2025
Quantity recalled32 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0348-2025
FDA event ID
97242
Recalling firm
Jalux America, El Segundo, CA
Brand
Lespoir
Classification
Class I
Status
Terminated
Recall initiated
10 Jul 2025
FDA classified
28 Jul 2025
Reported
6 Aug 2025
Type
Voluntary: Firm initiated
Customers notified by
Other
Reason category
Undeclared Milk
Product category
Cookies

Timeline

10 Jul 2025Recall initiated by company
28 Jul 2025Classified by FDA+18 days
6 Aug 2025Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared Milk

Product as listed by the FDA

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

Where it was distributed

CA, IL, WA

CaliforniaIllinoisWashington

Questions about this recall

Is Lespoir cookie recalled?

Yes. Jalux America recalled Lespoir cookie on 10 Jul 2025. The recall is Class I and its status is Terminated. Recall number H-0348-2025.

Why was it recalled?

Undeclared Milk

Which lots are affected?

Best Before date: September 26, 2025

Where was it sold?

CA, IL, WA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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.

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