Food Recall Check
Class I · High risk Terminated Initiated Mar 26, 2014 (13 years ago)

Oscar's Smoke House Plain Cheddar Spread recall

Recalled by Oscar's Hickory House, Inc. · Warrensburg, NY, United States

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

Why it was recalled

Products were recalled due to potential Listeria monocytogenes contamination.

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

OSCAR'S SMOKE HOUSE PLAIN CHEDDAR SPREAD, NET WT 7 OZS, keep refrigerated. Distributed by: Oscar's Smoke House Warrensburg, NY 12885.

Quantity: 1,131 units

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 numbers: 719-959

Where it was sold

Nationwide.

New York

FDA's distribution note: Nationwide through internet mail order sales and to NY retail stores

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
Oscar's Hickory House, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 26, 2014
In FDA report of
Oct 29, 2014
Terminated
Jun 8, 2018
FDA recall number
F-0070-2015 · event 67843
Official record
FDA enforcement report search

Also recalled with it (10 more products)

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