El Marwa for Preserving and Freezing Vegetables and Fruits

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

Refusal charges, in plain English

• 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.

• PESTICIDE1 refused line

  Pesticide chemical residue

  The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

Questions about El Marwa for Preserving and Freezing Vegetables and Fruits

Is El Marwa for Preserving and Freezing Vegetables and Fruits on an FDA import alert?

Yes. As of October 26, 2026, El Marwa for Preserving and Freezing Vegetables and Fruits is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for spinach; FDA published the listing on October 27, 2022.

Has FDA refused shipments from El Marwa for Preserving and Freezing Vegetables and Fruits?

Yes. FDA refused 1 shipment line from El Marwa for Preserving and Freezing Vegetables and Fruits on July 5, 2022. The most recent, on July 5, 2022, was spinach (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).

Why did FDA refuse El Marwa for Preserving and Freezing Vegetables and Fruits's shipments?

The most frequent charges are NUTRIT LBL (nutrition information missing from label, 1 line) and PESTICIDE (pesticide chemical residue, 1 line).

What is El Marwa for Preserving and Freezing Vegetables and Fruits's FEI number?

El Marwa for Preserving and Freezing Vegetables and Fruits's FDA Establishment Identifier (FEI) is 3007052955.

Can shipments from El Marwa for Preserving and Freezing Vegetables and Fruits still enter the U.S.?

Shipments of spinach from El Marwa for Preserving and Freezing Vegetables and Fruits can be detained without physical examination under Import Alert 99-08; 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).