Gaiser's European Style Provisions product recalled over undeclared pork

Recall date

June 27, 2025

Source

U.S. Department of Agriculture (USDA FSIS)

Official notice title

Gaiser's European Style Provisions Inc. Recalls Ready-To-Eat Meat and Poultry Bologna Products Due to Misbranding

Recall number

024-2025

FDA classification

Class III

Brand / firm

Gaiser's European Style Provisions Inc.

Sold / distributed

Nationwide

Why it was recalled

Misbranding

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

WASHINGTON, June 27, 2025 – Gaiser's European Style Provisions Inc., a Union, N.J., establishment, is recalling approximately 143,416 pounds of ready-to-eat bologna due to misbranding, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The various bologna products subject to recall contain meat or poultry source materials that are not declared on the product labels. The ready-to-eat bologna items were produced between March 20 and June 20, 2025. The following products are subject to recall [ view labels ]: Vacuum-packed packages of “FAMILY TREE BOLOGNA VEAL” containing undeclared pork. Plastic-wrapped packages of “BABUSHKA’S RECIPE CHICKEN BOLOGNA” containing undeclared pork. Plastic-wrapped packages of “FANCY BOLOGNA” labeled with pork as an ingredient but containing undeclared beef and chicken. Vacuum-packed packages of “GAISERS RUSSIAN BRAND DOKTORSKAYA BOLOGNA” containing undeclared beef. Plastic-wrapped packages of “GAISERS BOLOGNA VEAL” containing undeclared chicken and pork. Plastic-wrapped packages of “GAISERS TURKEY BOLOGNA” containing undeclared chicken and pork. Plastic-wrapped packages of “CHICKEN BOLOGNA KYPOYKA PABA” containing undeclared pork. The products subject to recall were distributed to wholesale and retail locations nationwide and bare establishment number “EST. 5385” inside the USDA mark of inspection on the product labels. Some products would have been weighed, wrapped, and labeled in retail store locations at the time of purchase. The problem was discovered when FSIS was notified by the Office of Inspector General (OIG) of a complaint received through the OIG’s hotline. FSIS investigated the complaint and determined that the products contained source materials that were not declared on the label. Although FSIS does not expect any adverse health effects for Class III recalled products and there have been no confirmed reports of adverse reactions due to consumption of these products, anyone concer…