Food Recall Check
Class I · High risk Terminated Initiated Sep 10, 2012 (14 years ago)

Ricotta Salata Frescolina Brand Soft Cheese recall

Recalled by Floyd Peterson Company Inc. · Auburn, WA, United States

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

Why it was recalled

Ricotta Salata Frescolina Brand Cheese is recalled due to the potential contamination with Listeria monocytonenes.

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

Ricotta Salata Frescolina Brand Soft Cheese. Product is packaged in a retail package, wedge shaped, size ranges from 6-7 oz. The product is labeled in parts: "***Frescolina Ricotta Salata MARTE***IMPORTED BY FOREVER CHEESE,NY 11106***PRODUCT OF ITALY***"

Quantity: total 390 lbs

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.

manufacturer codes 7022, 7212, 7272 and 7432.

Where it was sold

Oregon Washington

FDA's distribution note: Product distributed to distributors, retailers, and restaurants in Oregon and Washington.

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
Floyd Peterson Company Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 10, 2012
In FDA report of
Oct 24, 2012
Terminated
Oct 31, 2012
FDA recall number
F-0122-2013 · event 63217
Official record
FDA enforcement report search

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