RecallHawk
Class I Recall

Authentic Fresh to You Deluxe Triple Decker Club Net Wt. 8.8oz (254g). Product packaged in a plastic PET container.

MG Foods Middletown

Summary

The FDA issued a Class I for Authentic Fresh to You Deluxe Triple Decker Club Net Wt. 8.8oz (254g). Product p by MG Foods Middletown. Reason: Undeclared egg.

Details

Source

Food Recall

External ID

F-0858-2024

Action Date

2024-02-14

Status

Terminated

Category

food

Product Description

Authentic Fresh to You Deluxe Triple Decker Club Net Wt. 8.8oz (254g). Product packaged in a plastic PET container.

Lot/Code Info: MGF9719 Fresh Thru 01/27/24 MGF9719 Fresh Thru 01/30/24

Quantity Affected: 852 units

Reason for Recall

Undeclared egg

Distribution

Distributed to distributors in PA, NJ, MD and NY. Product is then sold in canteen and vending machines.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-25

Company

MG Foods Middletown

Middletown, PA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (MG Foods Middletown) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does MG Foods Middletown have FDA actions?

This is the only FDA action we have on record for MG Foods Middletown in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0858-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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