RecallHawk
Class II Recall

COCKTAIL SAUCE Ingredients: Ketchup horseradish, vinegar Worcestershire sauce garlic salt Net Wt 8 oz WASHINGTON CRAB Ca

Washington Crab & Seafood Company, Inc.

Summary

The FDA issued a Class II for COCKTAIL SAUCE Ingredients: Ketchup horseradish, vinegar Worcestershire sauce ga by Washington Crab & Seafood Company, Inc.. Reason: Undeclared fish and soy..

Details

Source

Food Recall

External ID

F-0927-2023

Action Date

2023-05-31

Status

Ongoing

Category

food

Product Description

COCKTAIL SAUCE Ingredients: Ketchup horseradish, vinegar Worcestershire sauce garlic salt Net Wt 8 oz WASHINGTON CRAB Carolina seafood

Lot/Code Info: Sell by date 4/14/22-10/04/23

Quantity Affected: 52/8 oz cups

Reason for Recall

Undeclared fish and soy.

Distribution

Product was shipped to NC & SC.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-14

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 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Washington Crab & Seafood Company, Inc. has 4 FDA actions in our database, including 4 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 (Washington Crab & Seafood 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 Washington Crab & Seafood Company, Inc. have FDA actions?

Washington Crab & Seafood Company, Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0927-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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