CLASS I Food recall · Reported 10 Aug 2022 · FDA Enforcement Report

Double Fudge Blend (04-3118-35) recalled by Pecan Deluxe Candy Company

Pecan Deluxe Candy Company is recalling Double Fudge Blend (04-3118-35), distributed in Missouri. The recall was initiated on 12 Jul 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes04-2118-35 lot 22118
Quantity recalled1400 pounds

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-1513-2022
FDA event ID
90598
Recalling firm
Pecan Deluxe Candy Company, Dallas, TX
Classification
Class I
Status
Terminated
Recall initiated
12 Jul 2022
FDA classified
1 Aug 2022
Reported
10 Aug 2022
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Peanuts
Product category
Chocolate

Timeline

12 Jul 2022Recall initiated by company
1 Aug 2022Classified by FDA+20 days
10 Aug 2022Published 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

Potential to contain undeclared peanuts

Product as listed by the FDA

Double Fudge Blend (04-3118-35) 35lbs. (15.88 KG) packaged in a blue plastic bag (ZZ500) inside a printed corrugated box (ZZ240),

Where it was distributed

MO

Missouri

Questions about this recall

Is Double Fudge Blend (04-3118-35) recalled?

Yes. Pecan Deluxe Candy Company recalled Double Fudge Blend (04-3118-35) on 12 Jul 2022. The recall is Class I and its status is Terminated. Recall number F-1513-2022.

Why was it recalled?

Potential to contain undeclared peanuts

Which lots are affected?

04-2118-35 lot 22118

Where was it sold?

MO

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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