Tianjin Zhanhe Vegetable Co.,

3 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• ALLERGEN1 refused line

  Major food allergen not declared

  The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.

• INCONSPICU1 refused line

  Required information not conspicuous

  Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

• LIST INGRE1 refused line

  Ingredients not listed

  The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

• NUTRIT LBL1 refused line

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Tianjin Zhanhe Vegetable Co.,

Is Tianjin Zhanhe Vegetable Co., on an FDA import alert?

Yes. As of October 26, 2026, Tianjin Zhanhe Vegetable Co., is on the red list of FDA Import Alert 99-22, “Undeclared or mislabeled major food allergens”, for walnut bun; FDA published the listing on November 4, 2019.

Has FDA refused shipments from Tianjin Zhanhe Vegetable Co.,?

Yes. FDA refused 1 shipment line from Tianjin Zhanhe Vegetable Co., on November 20, 2019. The most recent, on November 20, 2019, was other bakery products, n.e.c., charged as LIST INGRE (ingredients not listed).

Why did FDA refuse Tianjin Zhanhe Vegetable Co.,'s shipments?

The most frequent charges are ALLERGEN (major food allergen not declared, 1 line) and INCONSPICU (required information not conspicuous, 1 line).

What is Tianjin Zhanhe Vegetable Co.,'s FEI number?

Tianjin Zhanhe Vegetable Co.,'s FDA Establishment Identifier (FEI) is 3011148198.

Can shipments from Tianjin Zhanhe Vegetable Co., still enter the U.S.?

Shipments of walnut bun from Tianjin Zhanhe Vegetable Co., can be detained without physical examination under Import Alert 99-22; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).