Snoqualmie Berry Sorbet Recalled for Potential Listeria Contamination
Snoqualmie Gourmet Ice Cream is recalling Berry Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 1-gallon trays.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class I, which mandates a minimum severity score of 4 per the rubric. Additionally, Listeria monocytogenes is a high-risk pathogen.
Plain-English summary
Snoqualmie Gourmet Ice Cream is recalling Berry Sorbet sold in 1-gallon plastic trays. The recall is due to the potential for the product to be contaminated with Listeria monocytogenes. The product does not have a UPC code.
The affected units were produced between January 1, 2014, and December 15, 2014. A total of 11 trays were distributed nationwide. The source text does not specify specific states or retail locations where the product was sold.
Consumers who have purchased this product should check their freezers for Berry Sorbet in 1-gallon trays with production dates within the specified range. If found, consumers should discard the product or return it to the place of purchase. The source text does not provide specific instructions for disposal or refund procedures beyond the standard recall context.
The recalled product
- Product
- Berry Sorbet, sold under Snoqualmie brand. Product is sold in 1 gallon plastic trays. No UPC.
- Manufacturer
- Snoqualmie Gourmet 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 (3)
- Production date: January 1
- 2014 through December 15
- 2014.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 117 recalled by Snoqualmie Gourmet 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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