RecallHawk
Class II Recall

5912MOD-CAU Pre-Blend, item #991819, is a dry blend. Ingredients consist of Tapioca Starch, Long Grain Rice Flour, Chees

Bridgewell Agribusiness LLC

Summary

The FDA issued a Class II for 5912MOD-CAU Pre-Blend, item #991819, is a dry blend. Ingredients consist of Tapi by Bridgewell Agribusiness LLC. Reason: Foreign material appears to be white nylon or other plastic thread was found in product..

Details

Source

Food Recall

External ID

F-0563-2025

Action Date

2025-02-19

Status

Terminated

Category

food

Product Description

5912MOD-CAU Pre-Blend, item #991819, is a dry blend. Ingredients consist of Tapioca Starch, Long Grain Rice Flour, Cheese Powder [Cheddar Cheese (Cultured Pasteurized Milk, Salt, Enzymes), Disodium Phosphate, Salt], Rice Starch, Sugar, Salt, Encapsulated Baking Soda (Sodium Bicarbonate, Hydrogenated Soybean, Palm, and/or Cottonseed Oils), Sodium Aluminum Phosphate, Dehydrated Garlic, and Seasoning (Spices, Dehydrated Garlic and Onion, Sunflower Oil). Product of USA. Distributed by Bridgewell Agribusiness LLC 12420 SE Carpenter Drive, Clackamas, OR 97015. Product is packaged in 50lbs. kraft bag and it is intended for further processing.

Lot/Code Info: Lot Code: 220349 Expire on November 18, 2025

Quantity Affected: 792 bags (50.34 lbs. per bag)

Reason for Recall

Foreign material appears to be white nylon or other plastic thread was found in product.

Distribution

Distributed in NY only.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-01-23

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Bridgewell Agribusiness LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Bridgewell Agribusiness LLC have FDA actions?

This is the only FDA action we have on record for Bridgewell Agribusiness LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0563-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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