RecallHawk
Class II Recall

Egg salad sandwich packaged in clamshell for individual sale. 7.22oz (205g) UPC 766375938415

The Coastal Companies DBA Hearn Kirkwood

Summary

The FDA issued a Class II for Egg salad sandwich packaged in clamshell for individual sale. 7.22oz (205g) UPC by The Coastal Companies DBA Hearn Kirkwood. Reason: Tuna salad sandwich was mislabeled as an egg salad sandwich. There is an undeclared allergen of fish (Tuna)..

Details

Source

Food Recall

External ID

F-1132-2024

Action Date

2024-04-17

Status

Terminated

Category

food

Product Description

Egg salad sandwich packaged in clamshell for individual sale. 7.22oz (205g) UPC 766375938415

Lot/Code Info: Use By Date of 03/23/2024

Quantity Affected: 551 units

Reason for Recall

Tuna salad sandwich was mislabeled as an egg salad sandwich. There is an undeclared allergen of fish (Tuna).

Distribution

Product was sold to institutions, hospitals and retailers in DC, FL, MA, MD, MI, NJ, NY, OH, PA, VA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-23

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

The Coastal Companies DBA Hearn Kirkwood has 7 FDA actions in our database, including 7 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 (The Coastal Companies DBA Hearn Kirkwood) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does The Coastal Companies DBA Hearn Kirkwood have FDA actions?

The Coastal Companies DBA Hearn Kirkwood has 7 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1132-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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