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