CLASS II ONGOING Food recall · Reported 31 May 2023 · FDA Enforcement Report

Blue Crab Dip Ingredients: Blue Crabmeat, cream cheese recalled

Washington Crab & Seafood is recalling Blue Crab Dip Ingredients: Blue Crabmeat, cream cheese, vidalia onion, salt, paprika, and, distributed in North Carolina, South Carolina. The recall was initiated on 14 Apr 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSell by Date 11/4/22-4/24/23
Quantity recalled3469/8 oz cups

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0926-2023
FDA event ID
92122
Recalling firm
Washington Crab & Seafood, Washington, NC
Classification
Class II
Status
Ongoing
Recall initiated
14 Apr 2023
FDA classified
23 May 2023
Reported
31 May 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Milk
Product category
Dips & Spreads

Timeline

14 Apr 2023Recall initiated by company
23 May 2023Classified by FDA+39 days
31 May 2023Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared milk

Product as listed by the FDA

BLUE CRAB DIP 8 oz Ingredients: Blue Crabmeat, cream cheese, vidalia onion, salt, paprika, and spice WASHINGTON CRAB Carolina Seafood

Where it was distributed

Product was shipped to NC & SC.

North CarolinaSouth Carolina

Questions about this recall

Why was it recalled?

Undeclared milk

Which lots are affected?

Sell by Date 11/4/22-4/24/23

Where was it sold?

Product was shipped to NC & SC.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 92122

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