RecallHawk
Class II Recall

DELI CAROLINA STYLE MUSTARD BBQ SAUCE, 2 oz (57g), plastic cup, 96 cups/case, store in ambient temperatures

Ventura Foods Llc

Summary

The FDA issued a Class II for DELI CAROLINA STYLE MUSTARD BBQ SAUCE, 2 oz (57g), plastic cup, 96 cups/case, st by Ventura Foods Llc. Reason: Undeclared fish (anchovy) allergen.

Details

Source

Food Recall

External ID

F-0713-2024

Action Date

2024-01-24

Status

Terminated

Category

food

Product Description

DELI CAROLINA STYLE MUSTARD BBQ SAUCE, 2 oz (57g), plastic cup, 96 cups/case, store in ambient temperatures

Lot/Code Info: B31423 Use By: APR 08 24B Manufacture Date: 11/10/2023 Use By: APR 08 24B

Quantity Affected: 392 cases

Reason for Recall

Undeclared fish (anchovy) allergen

Distribution

Products are distributed at the Wholesale (Distribution) level. U.S. distribution to GA and FL. No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-04

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 81 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Ventura Foods Llc has 7 FDA actions in our database, including 7 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Ventura Foods Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Ventura Foods Llc have FDA actions?

Ventura Foods Llc has 7 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0713-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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