CLASS I Food recall · Reported 27 Dec 2017 · FDA Enforcement Report

Choceur Dark Chocolate Bars/case recalled by Aldi

Aldi is recalling Choceur Dark Chocolate Bars/case, distributed in 12 states. The recall was initiated on 5 Dec 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesThe best-by date is July 24, 2018
Quantity recalled93,500 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-0555-2018
FDA event ID
78712
Recalling firm
Aldi, Batavia, IL
Brand
Choceur
Classification
Class I
Status
Terminated
Recall initiated
5 Dec 2017
FDA classified
8 Jan 2018
Reported
27 Dec 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Tree Nuts
Product category
Chocolate

Timeline

5 Dec 2017Recall initiated by company
27 Dec 2017Published in enforcement report+22 days
8 Jan 2018Classified by FDA+12 days

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

Reason for recall

ALDI has voluntarily recalled Choceur Dark Chocolate Bars due to the potential presence of almond pieces, which are an undeclared treenut allergen.

Product as listed by the FDA

Choceur Dark Chocolate Bars, 5.29 oz., 20 units/case

Where it was distributed

Domestic: OH, IN, WI, NY, MI, IL, MD, CT, GA, FL, TX No foreign or VA/DOD

ConnecticutFloridaGeorgiaIllinoisIndianaMarylandMichiganNew YorkOhioTexasVirginiaWisconsin

Stores named: Aldi

Questions about this recall

Why was it recalled?

ALDI has voluntarily recalled Choceur Dark Chocolate Bars due to the potential presence of almond pieces, which are an undeclared treenut allergen.

Which lots are affected?

The best-by date is July 24, 2018

Where was it sold?

Domestic: OH, IN, WI, NY, MI, IL, MD, CT, GA, FL, TX No foreign or VA/DOD

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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