CLASS II Food recall · Reported 18 Feb 2026 · FDA Enforcement Report

Smoked Grouper Dip with tamper proof lid tub recalled by Island Crab

Island Crab is recalling Smoked Grouper Dip with tamper proof lid tub, distributed in Florida. The recall was initiated on 8 Jan 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesExpiration Date 01/20/2026 Expiration Date 01/26/2026
Quantity recalled23 - 7 lb plastic tub

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
H-0494-2026
FDA event ID
98334
Recalling firm
Island Crab, St James City, FL
Classification
Class II
Status
Terminated
Recall initiated
8 Jan 2026
FDA classified
11 Feb 2026
Reported
18 Feb 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Dips & Spreads

Timeline

8 Jan 2026Recall initiated by company
11 Feb 2026Classified by FDA+34 days
18 Feb 2026Published in enforcement report+7 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, Eggs, Sodium metabisulfite

Product as listed by the FDA

Smoked Grouper Dip 7lb plastic tub with tamper proof lid 1/7lb tub per case. Keep Refrigerated.

Where it was distributed

Florida

Florida

Questions about this recall

Why was it recalled?

Undeclared Milk, Eggs, Sodium metabisulfite

Which lots are affected?

Expiration Date 01/20/2026 Expiration Date 01/26/2026

Where was it sold?

Florida

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.

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