Food Recall Check
Class III · Low risk Terminated Initiated Jun 5, 2013 (13 years ago)

Kenton's Cheese CO recall

Recalled by Kenton Burr · Trumansburg, NY, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Kenton's Cheese Co. is recalling Bianco A Soft Brie-Style Cheese due to E.coli contamination. Consumers who have purchased Bianco-Brie from Kenton's Cheese Co. between May 9, 2013 and May 19, 2013 listed with Batch number 13064, are urged to return the product to Kenton's Cheese Co. 5939 Burr Road Trumansburg, NY 14886. Questions may be directed to Kenton Burr (607) 592-0746 or via e-mail [email protected]. A full refund will be provided by Kenton's Cheese Co.

Pathogen: E. coli

Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.

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

KENTON'S CHEESE CO. Bianco A soft Brie-Style cheese Aged at least 60 days, Net Wt. 8 oz wheel. Distributed by Kenton's Cheese Company 5939 Burr Rd. Trumansburg, NY 14886.

Quantity: 200 wheels

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.

Batch: 13064

Where it was sold

New York

FDA's distribution note: New York State (Fingerlakes region)

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
Kenton Burr
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 5, 2013
In FDA report of
Jul 24, 2013
Terminated
Feb 16, 2017
FDA recall number
F-1716-2013 · event 65427
Official record
FDA enforcement report search

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