5912MOD-CAU Pre-Blend recall
Recalled by Bridgewell Agribusiness LLC · Clackamas, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Foreign material appears to be white nylon or other plastic thread was found in product.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
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.
Quantity: 792 bags (50.34 lbs. per bag)
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot Code: 220349 Expire on November 18, 2025
Where it was sold
New York
FDA's distribution note: Distributed in NY only.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Bridgewell Agribusiness LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 23, 2025
- In FDA report of
- Feb 19, 2025
- Terminated
- Apr 3, 2025
- FDA recall number
- F-0563-2025 · event 96180
- Official record
- FDA enforcement report search