Mon Sire Brie
Reason The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
Laubscher Cheese Co recall
Recalled by Laubscher Cheese Company, Ltd. · Mercer, PA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Laubscher Cheese Company, LTD , has initiated a recall of Shredded Cheese, because samples of the shredded cheese were found 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
Laubscher Cheese Co.; Shredded Cheese; Net Wt. 5 LBS. and 2 LBS.,Cryovac sealed plastic bags, Distributed By: Laubscher Cheese Co. Mercer, PA 16137
Quantity: 1,617,420 lbs of Shredded Cheese
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.
October 9 2019 - November 25 2019 - Pack Date
Where it was sold
FDA's distribution note: All product shipped with in the United States
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
- Laubscher Cheese Company, Ltd.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 29, 2019
- In FDA report of
- Feb 12, 2020
- Terminated
- Jun 27, 2022
- FDA recall number
- F-0601-2020 · event 84386
- Official record
- FDA enforcement report search
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