BLUE CRAB DIP 8 oz Ingredients: Blue Crabmeat, cream cheese, vidalia onion, salt, paprika, and spice WASHINGTON CRAB Car
Summary
The FDA issued a Class II for BLUE CRAB DIP 8 oz Ingredients: Blue Crabmeat, cream cheese, vidalia onion, salt by Washington Crab & Seafood Company, Inc.. Reason: Undeclared milk.
Details
Source
Food Recall
External ID
F-0926-2023
Action Date
2023-05-31
Status
Ongoing
Category
food
Product Description
BLUE CRAB DIP 8 oz Ingredients: Blue Crabmeat, cream cheese, vidalia onion, salt, paprika, and spice WASHINGTON CRAB Carolina Seafood
Lot/Code Info: Sell by Date 11/4/22-4/24/23
Quantity Affected: 3469/8 oz cups
Reason for Recall
Undeclared milk
Distribution
Product was shipped to NC & SC.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-14
Company
Washington, NC
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-0926-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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