Kerry BATTER G3665 Recalled for Nylon String Foreign Material
Kerry, Inc. is recalling BATTER G3665 because it contains foreign material (nylon string). The product was distributed to manufacturers and food service distributors in nine US states.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically involves a situation where use of the product could cause temporary or medically reversible health consequences. The hazard is a foreign material (nylon string), which is a physical hazard rather than a high-risk biological pathogen or severe chemical contaminant, fitting the Moderate severity criteria for low-risk contamination or voluntary precautionary recalls.
Plain-English summary
Kerry, Inc. is recalling BATTER G3665, Item Number G3665.49, Net Wt. 50 lb, because the product contains foreign material (nylon string). The product is distributed by Kerry Ingredients & Flavours in Beloit, WI.
The recall affects 1,770 units of the product. It was distributed to manufacturers and food service distributors in the following US states: AL, AR, CA, FL, GA, MO, OH, OK, TX, and WI. The specific codes associated with the recalled product are 0617987103, 0703987104, and 0722987103.
Consumers and businesses who have purchased or received this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- BATTER G3665, Item Number G3665.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
- Manufacturer
- Kerry, Inc
- Category
- Food — Food Ingredient
- Hazard
- Affected units
- 1,770
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)
- 0617987103
- 0703987104
- and 0722987103
Distribution
Part of a larger recall action
This product is one of 58 recalled by Kerry, Inc 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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