Mehsana District Co-Operative Milk Producers Union LTD

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.

• FALSE1 refused line

  False or misleading labeling

  The labeling appeared to be false or misleading in some particular.

• HEALTH C1 refused line

  Unauthorized nutrient content or health claim

  The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.

Questions about Mehsana District Co-Operative Milk Producers Union LTD

Is Mehsana District Co-Operative Milk Producers Union LTD on an FDA import alert?

Yes. As of October 26, 2026, Mehsana District Co-Operative Milk Producers Union LTD is on the red list of FDA Import Alert 99-22, “Undeclared or mislabeled major food allergens”, for vegetable cooking oil/cow ghee; FDA published the listing on September 22, 2023.

Has FDA refused shipments from Mehsana District Co-Operative Milk Producers Union LTD?

Yes. FDA refused 1 shipment line from Mehsana District Co-Operative Milk Producers Union LTD on September 6, 2022. The most recent, on September 6, 2022, was butter oil, charged as FALSE (false or misleading labeling).

Why did FDA refuse Mehsana District Co-Operative Milk Producers Union LTD's shipments?

The most frequent charges are ALLERGEN (major food allergen not declared, 1 line) and FALSE (false or misleading labeling, 1 line).

What is Mehsana District Co-Operative Milk Producers Union LTD's FEI number?

Mehsana District Co-Operative Milk Producers Union LTD's FDA Establishment Identifier (FEI) is 3004572173.

Can shipments from Mehsana District Co-Operative Milk Producers Union LTD still enter the U.S.?

Shipments of vegetable cooking oil/cow ghee from Mehsana District Co-Operative Milk Producers Union LTD 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).