Food Recall Check
Class I · High risk Terminated Initiated Sep 30, 2019 (7 years ago)

Consider Bardwell Farm Dorset cheese PLU code 97776 sliced and… recall

Recalled by Whole Foods Market · Austin, TX, United States

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

Why it was recalled

Potential to 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

Consider Bardwell Farm Dorset cheese PLU code 97776 sliced and wrapped in plastic cling with Whole Foods Market scale label applied

Quantity: 14.90 pounds

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.

Whole Foods Market scale label, identifiable by PLU code 97776 with sell-by dates through 10/30/2019.

Where it was sold

Connecticut Massachusetts Maine New Hampshire New Jersey New York Rhode Island

FDA's distribution note: NORTH ATLANTIC AND NORTHEAST WHOLE FOODS MARKET STORES: CT, MA, ME, NH, NJ, NY, RI

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
Whole Foods Market
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 30, 2019
In FDA report of
Oct 30, 2019
Terminated
Jan 14, 2020
FDA recall number
F-0129-2020 · event 83931
Official record
FDA enforcement report search

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