Johnvince Foods

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

Refusal charges, in plain English

• 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.

• 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 Johnvince Foods

Is Johnvince Foods on an FDA import alert?

Yes. As of October 25, 2026, Johnvince Foods is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for organic red quinoa; FDA published the listing on December 26, 2019.

Has FDA refused shipments from Johnvince Foods?

Yes. FDA refused 2 shipment lines from Johnvince Foods between April 3, 2017 and September 22, 2020. The most recent, on September 22, 2020, was quinoa seed (edible seed), charged as PESTICIDE (pesticide chemical residue).

Why did FDA refuse Johnvince Foods's shipments?

The most frequent charges are LIST INGRE (ingredients not listed, 1 line) and NUTRIT LBL (nutrition information missing from label, 1 line).

When was Johnvince Foods last inspected by FDA?

FDA's most recent inspection of Johnvince Foods with a final classification is dated May 31, 2011 and was classified VAI (Voluntary Action Indicated).

What is Johnvince Foods's FEI number?

Johnvince Foods's FDA Establishment Identifier (FEI) is 3000999705.

Can shipments from Johnvince Foods still enter the U.S.?

Shipments of organic red quinoa from Johnvince Foods 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).