(LOOTPRESS) – West Virginia pet owners should be aware that Blue Ridge Beef has recalled 5,700 pounds of its 2 lb. log Natural Mixdue to Salmonella contamination.
The affected product has Lot # N25/12/31 (stamped on the clips at the ends of the packaging) and UPC# 854298001054.
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Health Risks for Pets and Humans
Salmonella poses a risk to both animals and humans. Pets infected with Salmonella may experience lethargy, diarrhea (which may be bloody), vomiting, fever, and abdominal pain.
Some infected pets may appear healthy but can still spread the bacteria. If your pet has consumed the recalled food and shows any of these symptoms, contact a veterinarian immediately.
For humans, handling contaminated pet food can lead to nausea, vomiting, diarrhea, fever, and abdominal cramps. In rare cases, more severe complications like arterial infections, arthritis, and endocarditis can occur.
Anyone who develops symptoms after contact with the recalled product should seek medical attention.
Recall Details
The North Carolina Department of Agriculture tested the product on January 8, 2025, and found it positive for Salmonella.
The FDA notified Blue Ridge Beef on January 27, 2025, confirming the contamination.
The product was distributed between January 3 and January 24, 2025, and was sold primarily in retail stores across Virginia, Maryland, Pennsylvania, Connecticut, Massachusetts, New York, Tennessee, and Rhode Island.
While West Virginia was not listed as a primary distribution area, residents who have purchased pet food across state lines should check their products.
What to Do If You Have the Recalled Product
- Do not feed the recalled food to pets or other animals.
- Return it to the place of purchase or dispose of it in a way that prevents access by children, pets, and wildlife.
- Clean and sanitize pet food bowls, storage containers, and any surfaces that came in contact with the product.
- Wash hands thoroughly after handling recalled pet food.
For more information, contact Blue Ridge Beef at blueridgebeefnc@yahoo.com or 704-873-2072.
This recall is being conducted with the knowledge of the FDA.
