RecallHawk
Class I Recall

DOUX SOUTH PICKLES EAT WITH A SOUTHERN ACCENT BAKKAVOR CURRY CAULIFLOWER 5 GALLON

Doux South Specialties LLC

Summary

The FDA issued a Class I for DOUX SOUTH PICKLES EAT WITH A SOUTHERN ACCENT BAKKAVOR CURRY CAULIFLOWER 5 GALLO by Doux South Specialties LLC. Reason: The firm received a positive test result for Listeria monocytogenes for the product..

Details

Source

Food Recall

External ID

F-1060-2022

Action Date

2022-05-25

Status

Terminated

Category

food

Product Description

DOUX SOUTH PICKLES EAT WITH A SOUTHERN ACCENT BAKKAVOR CURRY CAULIFLOWER 5 GALLON

Lot/Code Info: LOT: 05510822 BEST BY: 7/21/22

Quantity Affected: 145/5 gallon pails

Reason for Recall

The firm received a positive test result for Listeria monocytogenes for the product.

Distribution

Product was shipped to CA & NC

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-19

Company

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

How often does Doux South Specialties LLC have FDA actions?

This is the only FDA action we have on record for Doux South Specialties LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1060-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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