CLASS I Food recall · Reported 19 Aug 2020 · FDA Enforcement Report

Kouign-Amann Pastry available recalled by Whole Foods Market

Whole Foods Market is recalling Kouign-Amann Pastry available with Whole Foods Market scale labels, a, distributed in 7 states. The recall was initiated on 24 Jul 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesPLU code 26739400000 and a sell through date of July 27, 2020
Quantity recalled102 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
F-1145-2020
FDA event ID
86118
Recalling firm
Whole Foods Market, Austin, TX
Classification
Class I
Status
Terminated
Recall initiated
24 Jul 2020
FDA classified
7 Aug 2020
Reported
19 Aug 2020
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Egg
Product category
Cakes & Pastries

Timeline

24 Jul 2020Recall initiated by company
7 Aug 2020Classified by FDA+14 days
19 Aug 2020Published in enforcement report+12 days

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

Reason for recall

Potential to contain undeclared eggs

Product as listed by the FDA

Kouign-Amann Pastry available in plastic clamshell 4-packs with Whole Foods Market scale labels, a PLU code 26739400000

Where it was distributed

Colorado, Kansas, Missouri, Nebraska, New Mexico, Texas and Utah.

ColoradoKansasMissouriNebraskaNew MexicoTexasUtah

Stores named: Whole Foods

Questions about this recall

Why was it recalled?

Potential to contain undeclared eggs

Which lots are affected?

PLU code 26739400000 and a sell through date of July 27, 2020

Where was it sold?

Colorado, Kansas, Missouri, Nebraska, New Mexico, Texas and Utah.

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 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.

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