Wilcox Premium Blueberry Crumble in 1.5QT, Quart, Pint, and 3 Gallon sizes
Summary
The FDA issued a Class I for Wilcox Premium Blueberry Crumble in 1.5QT, Quart, Pint, and 3 Gallon sizes by WILCOX ICE CREAM. Reason: Products may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0548-2024
Action Date
2023-12-20
Status
Completed
Category
food
Product Description
Wilcox Premium Blueberry Crumble in 1.5QT, Quart, Pint, and 3 Gallon sizes
Lot/Code Info: Best By/Sell By dates of 9/14/24 to 11/14/24
Quantity Affected: 19.31 Tons Total
Reason for Recall
Products may be contaminated with Listeria monocytogenes.
Distribution
VT, NH, MA, and NY.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-15
Company
East Arlington, VT
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 143 food recalls issued in the same week, part of 204 food-related FDA actions this month.
WILCOX ICE CREAM has 59 FDA actions in our database, including 59 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 (WILCOX ICE CREAM) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does WILCOX ICE CREAM have FDA actions?
WILCOX ICE CREAM has 59 FDA actions in our database, including 59 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0548-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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