Synear Foods USA product recalled over undeclared allergens

Recall date

May 31, 2026

Source

U.S. Department of Agriculture (USDA FSIS)

Official notice title

Synear Foods USA, LLC Recalls Frozen Pork and Crab Soup Dumpling Products Due to Misbranding and Undeclared Allergens

Recall number

007-2026

FDA classification

Class I

Brand / firm

Synear Foods USA, LLC

Sold / distributed

California, New Jersey, Washington

Why it was recalled

Misbranding; Unreported Allergens

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

WASHINGTON, May 31, 2026 – Synear Foods USA, LLC, a Chatsworth, Calif. establishment, is recalling approximately 71,603 pounds of frozen not-ready-to-eat (NRTE) pork and crab soup dumpling products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains peanut, a known allergen, which is not declared on the product label. The frozen NRTE pork and crab soup dumpling products were produced between October 15, 2025, and February 23, 2026. The following products are subject to recall [ view labels ]: 13.23-oz. plastic bag packages containing “Synear SUPREME SOUP DUMPLING PORK & CRAB” and “BEST BY” dates 15 OCT 2026, 10 NOV 2026, 23 DEC 2026, 26 JAN 2027, or 23 FEB 2027. 375-g. plastic bag packages containing “Synear SUPREME SOUP DUMPLING DUMPLINGS À LA SOUPE SUPRÊME PORK & CRAB PORC ET CRABE” with “Product of USA/Produit des E.-U” and best by dates 2026 OC 15 or 2027 JA 26. The products subject to recall bear establishment number “EST. 45942” inside the USDA mark of inspection. These items were shipped to retail locations in California, New Jersey, and Washington. These products were also exported to Canada. The problem was discovered by FSIS inspection personnel during a routine allergen verification task. FSIS personnel identified that the products were formulated with peanut oil, but peanuts were not declared on the finished product label. The establishment determined that a formulation change led to the mislabeling. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider. FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recall…