Food Recall Check
Class I · High risk Terminated Initiated Jun 9, 2017 (9 years ago)

Classic Delight Ham & Cheese recall

Recalled by Classic Delight Inc · St Marys, OH, United States

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

Why it was recalled

Product test positive for 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

Classic Delight Ham & Cheese Net Wt. 4.0 oz (113 g) Contains: Wheat, Soy, Milk Distributed by Classic Delight Inc., St. Marys, OH 45885 UPC 0 20018 03226 8

Quantity: 76cs/12/4 oz Sandwiches

Food: Cheese

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.

Lot # 7146; Item #: 3226-12

Where it was sold

California Ohio

FDA's distribution note: Product was shipped to the following sates: CA & OH

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. 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
Classic Delight Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 9, 2017
In FDA report of
Jul 26, 2017
Terminated
Jan 31, 2018
FDA recall number
F-0294-2017 · event 77511
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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