RecallHawk
Class I Recall

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

Pecan Deluxe Candy Company, Inc.

Summary

The FDA issued a Class I for Double Fudge Blend (04-3118-35) 35lbs. (15.88 KG) packaged in a blue plastic bag by Pecan Deluxe Candy Company, Inc.. Reason: Potential to contain undeclared peanuts.

Details

Source

Food Recall

External ID

F-1513-2022

Action Date

2022-08-10

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: 04-2118-35 lot 22118

Quantity Affected: 1400 pounds

Reason for Recall

Potential to contain undeclared peanuts

Distribution

MO

Type: Voluntary: Firm initiated

Recall Initiated: 2022-07-12

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 30 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Pecan Deluxe Candy Company, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Pecan Deluxe Candy Company, Inc. have FDA actions?

This is the only FDA action we have on record for Pecan Deluxe Candy Company, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1513-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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