Wilcox Premium Coffee Recalled Due to Listeria Contamination
Wilcox Premium Coffee products with Best By dates from September 14 to November 14, 2024, may be contaminated with Listeria monocytogenes. Products were distributed in Vermont, New Hampshire, Massachusetts, and New York.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class I recall for Listeria monocytogenes, a high-risk pathogen. However, no illnesses, injuries, or deaths are reported in the source material. The rubric specifies that high-risk pathogens without reported illness score at High (3) level.
Plain-English summary
Wilcox Ice Cream is recalling Wilcox Premium Coffee in multiple sizes, including 4-ounce cups (UPC 04372600403), pints, quarts, 1.5-quart containers, 1-gallon, and 3-gallon sizes. The total quantity under recall is 19.31 tons.
The products may be contaminated with Listeria monocytogenes, a bacterium that can cause serious illness.
The recalled products were distributed in Vermont, New Hampshire, Massachusetts, and New York. Affected items have Best By or Sell By dates from September 14, 2024, through November 14, 2024.
Consumers should not eat these products. Check your freezer for Wilcox Premium Coffee with the affected date range and discard any items found. Anyone concerned about possible exposure should consult a healthcare provider.
The recalled product
- Product
- Wilcox Premium Coffee; 4 oz Cup; UPC 04372600403; Wilcox Premium Coffee in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
- Manufacturer
- WILCOX ICE CREAM
- Category
- Food — Frozen Desserts
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All Sizes with Best By/Sell By dates of 9/14/24 to 11/14/24:
Distribution
Part of a larger recall action
This product is one of 59 recalled by WILCOX ICE CREAM under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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