RecallHawk
Class II Recall

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

ISLAND CRAB CORPORATION

Summary

The FDA issued a Class II for Smoked Grouper Dip 7lb plastic tub with tamper proof lid 1/7lb tub per case. Kee by ISLAND CRAB CORPORATION. Reason: Undeclared Milk, Eggs, Sodium metabisulfite.

Details

Source

Food Recall

External ID

H-0494-2026

Action Date

2026-02-18

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: Expiration Date 01/20/2026 Expiration Date 01/26/2026

Quantity Affected: 23 - 7 lb plastic tub

Reason for Recall

Undeclared Milk, Eggs, Sodium metabisulfite

Distribution

Florida

Type: Voluntary: Firm initiated

Recall Initiated: 2026-01-08

Company

ISLAND CRAB CORPORATION

St James City, FL

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

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 (ISLAND CRAB CORPORATION) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does ISLAND CRAB CORPORATION have FDA actions?

This is the only FDA action we have on record for ISLAND CRAB CORPORATION in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0494-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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