CLASS I Food recall · Reported 14 Feb 2024 · FDA Enforcement Report

Authentic Fresh to You Deluxe Triple Decker Club recalled

MG Foods Middletown is recalling Authentic Fresh to You Deluxe Triple Decker Club, distributed in Maryland, New Jersey, New York, Pennsylvania. The recall was initiated on 25 Jan 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesMGF9719 Fresh Thru 01/27/24 MGF9719 Fresh Thru 01/30/24
Quantity recalled852 units

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-0858-2024
FDA event ID
93897
Recalling firm
MG Foods Middletown, Middletown, PA
Classification
Class I
Status
Terminated
Recall initiated
25 Jan 2024
FDA classified
7 Feb 2024
Reported
14 Feb 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Egg
Product category
Other

Timeline

25 Jan 2024Recall initiated by company
7 Feb 2024Classified by FDA+13 days
14 Feb 2024Published 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 egg

Product as listed by the FDA

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

Where it was distributed

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

MarylandNew JerseyNew YorkPennsylvania

Questions about this recall

Why was it recalled?

Undeclared egg

Which lots are affected?

MGF9719 Fresh Thru 01/27/24 MGF9719 Fresh Thru 01/30/24

Where was it sold?

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

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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