The Recall Desk
ModerateFDA (Food)·F-2005-2019·Announced 2019-08-21

Kerry Ultimate Batter/Breader Recalled for Nylon String Foreign Material

Kerry, Inc. is recalling 210 bags of Ultimate Batter/Breader due to the presence of 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 and involves a foreign material (nylon string) without reported illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

Kerry, Inc. is voluntarily recalling 210 bags of Ultimate Batter/Breader, Item Number 30753158.49, Net Wt. 50 lb. The recall is being conducted because the product contains foreign material, specifically nylon string. The product is distributed by Kerry Ingredients & Flavours in Beloit, Wisconsin.

The affected product was distributed to manufacturers and food service distributors in the following US states: Alabama, Arkansas, California, Florida, Georgia, Missouri, Ohio, Oklahoma, Texas, and Wisconsin. The specific code associated with the recalled product is 0618987101.

Consumers and businesses who have purchased this product should stop using it and contact the recalling firm for further instructions. This recall is classified as Class II by the FDA, indicating a situation where there is a reasonable probability that the use of or exposure to the violative product may cause temporary or medically reversible adverse health consequences.

The recalled product

Product
Ultimate Batter/Breader, Item Number 30753158.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
Manufacturer
Kerry, Inc
Category
Food — Food Ingredients
Hazard
Affected units
210

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)

  • 0618987101

Distribution

Distributed in 10 states:

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.

See all 58 products in this recall →

Related recalls

Same manufacturer · Kerry, Inc

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Same hazard · foreign material

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