RecallHawk
Class III Recall

Peanut Brittle, Cashew Brittle, Pecan Brittle, Bacon Brittle, Nashville Hot Brittle 5 oz, 8 oz, 16oz and bulk packaging

Brittle Brothers LLC

Summary

The FDA issued a Class III for Peanut Brittle, Cashew Brittle, Pecan Brittle, Bacon Brittle, Nashville Hot Brit by Brittle Brothers LLC. Reason: Undeclared soy.

Details

Source

Food Recall

External ID

F-0353-2023

Action Date

2023-02-22

Status

Terminated

Category

food

Product Description

Peanut Brittle, Cashew Brittle, Pecan Brittle, Bacon Brittle, Nashville Hot Brittle 5 oz, 8 oz, 16oz and bulk packaging

Lot/Code Info: 012323-1-BAC, 012323-2-BAC, 012323-3-BAC. -12323-5-BAC 012423-1-PEA, 012423-2-PEA, 012423-3-PEA, 012423-4-PEA, 012423-5-PEA, 012423-6-PEA, 012523-1-PEA, 012523-2-PEA, 012523-3-PEA, 012523-4-PEA, 012523-5-PEA,

Quantity Affected: 300- 5 oz. bags of Brittle

Reason for Recall

Undeclared soy

Distribution

TN

Type: Voluntary: Firm initiated

Recall Initiated: 2023-01-28

Company

Brittle Brothers LLC

Goodlettsville, TN

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 18 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Brittle Brothers LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Brittle Brothers LLC have FDA actions?

This is the only FDA action we have on record for Brittle Brothers LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0353-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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