CLASS I Food recall · Reported 8 Nov 2017 · FDA Enforcement Report

Whole Foods Hand Pie Apple Cinnamon recalled by Whole Foods Market

Whole Foods Market is recalling Whole Foods Hand Pie Apple Cinnamon, distributed in Arizona, California, Nevada. The recall was initiated on 13 Oct 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesbest-by dates of October 15, 2017 and earlier
Quantity recalled34 units (3 packs)

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-0085-2018
FDA event ID
78301
Recalling firm
Whole Foods Market, Glendale, CA
Classification
Class I
Status
Terminated
Recall initiated
13 Oct 2017
FDA classified
30 Oct 2017
Reported
8 Nov 2017
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Allergens
Product category
Cakes & Pastries

Timeline

13 Oct 2017Recall initiated by company
30 Oct 2017Classified by FDA+17 days
8 Nov 2017Published 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 allergen; egg.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Whole Foods Hand Pie Apple Cinnamon 3 PK, NET WT 8 oz. PLU number 23646100000

Where it was distributed

U.S. distribution to the following: CA, AZ, and NV. No foreign distribution.

ArizonaCaliforniaNevada

Stores named: Whole Foods

Questions about this recall

Is Whole Foods Hand Pie Apple Cinnamon recalled?

Yes. Whole Foods Market recalled Whole Foods Hand Pie Apple Cinnamon on 13 Oct 2017. The recall is Class I and its status is Terminated. Recall number F-0085-2018.

Why was it recalled?

Undeclared allergen; egg.

Which lots are affected?

best-by dates of October 15, 2017 and earlier

Where was it sold?

U.S. distribution to the following: CA, AZ, and NV. No foreign distribution.

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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