Food Recall Check
Class I · High risk Terminated Initiated Dec 27, 2019 (7 years ago)

RTE bacon and eggs recall

Recalled by Cheesewich Factory · Hodgkins, IL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Eggs in RTE bacon and egg packet may contain Listeria Monocytogenes.

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

RTE bacon and eggs 3.6 oz package

Quantity: 2516 cases, 6793.2 lbs.

Food: Eggs

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

USE BY" dates 12/27/19, 1/3/20, 1/23/20, 1/30/20, 2/6/20, 2/14/20, 2/19/20 and 2/28/20 and lot codes 281191, 302191, 309191, 316191, 323191, 331191, 336191, 344191

Where it was sold

Illinois Michigan North Carolina

FDA's distribution note: The firm distributed product to 4 distribution centers, Dot Foods, IL, S. Abrahams, MI, KINEX, NC, and Lipari Foods, MI.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Cheesewich Factory
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 27, 2019
In FDA report of
Jan 22, 2020
Terminated
May 20, 2020
FDA recall number
F-0515-2020 · event 84641
Official record
FDA enforcement report search

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