D. J.'s Boudain, LLC:
<p><strong>WASHINGTON, Jan. 31, 2025</strong> – D.J.’s… recall
What to do
Do not eat, serve, or sell the affected product.
Confirm affected products and instructions on the official notice before acting.
Why it was recalled
Product Contamination
Recall details
- Product
- <p><strong>WASHINGTON, Jan. 31, 2025</strong> – D.J.’s Boudain, LLC, a Beaumont, Texas, establishment, is recalling approximately 17,720 pounds of boudain sausage link products that may be contaminated with foreign materials, specifically pieces of a pen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.</p> <p>The fresh and frozen boudain sausage link items were produced on January 23, 2025. A list of the products subject to recall can be found here: [<a href="https://www.fsis.usda.gov/sites/default/files/media_file/documents/Recall-004-2025-Product-List_0.pdf">view product list</a>]. The labels for the impacted products can be found here: [<a href="https://www.fsis.usda.gov/sites/default/files/food_label_pdf/2025-01/recall-004-2025-labels.pdf">view labels</a>].</p> <p>The products subject to recall bear establishment number “EST. 13246” inside the USDA mark of inspection. These items were shipped to distributor, restaurant, and retail locations in Louisiana, Mississippi, and Texas.</p> <p>The problem was discovered after the establishment received a consumer complaint involving the discovery of a piece of a pen while eating the Original Boudain sausage links product.</p> <p>There has been one reported oral injury associated with consumption of this product. FSIS has received no additional reports of injury or illness from consumption of these products. Anyone concerned about an injury should contact a healthcare provider. 
- Brand
- D. J.'s Boudain, LLC
- Recall announced
- January 31, 2025
- Status
- False
- Distribution
- RC-004-2025-Retail-List.pdf
- Products / lots
- recall-004-2025-labels.pdf
- Classification
- Class I — High - Class I
Read the complete notice
The agency notice is the source for product identifiers, distribution, and any changes to the recall.
Archive records are not a statement about a product's current safety.