Wicklow Gold Cheddar Nettle & Chive Cheese, 5.2 oz., plastic cryo-vac , 8 packages per case
Summary
The FDA issued a Class I for Wicklow Gold Cheddar Nettle & Chive Cheese, 5.2 oz., plastic cryo-vac , 8 packag by Abbey Specialty Foods. Reason: Product may have Listeria Monocytogenes..
Details
Source
Food Recall
External ID
F-0425-2025
Action Date
2025-01-22
Status
Terminated
Category
food
Product Description
Wicklow Gold Cheddar Nettle & Chive Cheese, 5.2 oz., plastic cryo-vac , 8 packages per case
Lot/Code Info: Wicklow Gold Cheddar Nettle & Chive /Batch 24192/ Item # 28472/sell by date 6/2/25.
Quantity Affected: 133 cases
Reason for Recall
Product may have Listeria Monocytogenes.
Distribution
The recalled product was distributed to the following states: MA, CO, OH
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-18
Company
Fairfield, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Abbey Specialty Foods has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Abbey Specialty Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Abbey Specialty Foods have FDA actions?
Abbey Specialty Foods has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0425-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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