Wicklow Gold Cheddar Nettle & Chive Cheese
Reason Product may have Listeria Monocytogenes.
Wicklow Gold Cheddar Tomato & Herb recall
Recalled by Abbey Specialty Foods · Fairfield, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may have 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
Wicklow Gold Cheddar Tomato & Herb, 5.2 oz., plastic cryo-vac , 8 packages per case
Quantity: 100 cases
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.
Wicklow Gold Cheddar Tomato & Herb/Batch 24175/ Item 28473/Sell by 6/2/25
Where it was sold
Colorado Massachusetts Ohio
FDA's distribution note: The recalled product was distributed to the following states: MA, CO, OH
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
- Abbey Specialty Foods
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 18, 2024
- In FDA report of
- Jan 22, 2025
- Terminated
- Feb 20, 2025
- FDA recall number
- F-0426-2025 · event 96077
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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