Dulces Kokito, SA de CV
FDA import alert and refusal historyTlaquepaque, MexicoFEI 3004971614
As of October 26, 2026, Dulces Kokito, SA de CV (Tlaquepaque, Mexico) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for coconut bar pineapple flavor; coconut bar candy white, published by FDA on January 24, 2018, and has 5 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-21 · red list
- Last import refusal
- Candy specialties, n.e.c. (without chocolate) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Dulces Kokito, SA de CV
7 records, newest first. Each line links to the FDA page it came from.
2026
2023
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2018
- Import refusalRefused, Soft candy with coconut, n.e.c. (without chocolate)SULFITELBLEntry BRQ-0212557-4Source
- Import alert listingListed on Import Alert 99-21red listCoconut Bar Pineapple Flavor; Coconut Bar Candy WhiteSource
2017
- Import refusalRefused, Candy bar or pieces (not caramel or fondant), soft, with coconut (without chocolate)UNSAFE COLEntry 8MH-0000813-2Source
- Import refusalRefused, Candy bar or pieces (not caramel or fondant), soft, with coconut (without chocolate)UNSAFE COLCOLOR LBLGEntry 918-4874547-6Source
- Import refusalRefused, Soft candy with coconut, n.e.c. (without chocolate)NUTRIT LBLEntry BRQ-0189204-2Source
Refusal charges, in plain English
- UNSAFE COL2 refused lines
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- 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.
- SULFITELBL1 refused line
SULFITELBL
Questions about Dulces Kokito, SA de CV
- Is Dulces Kokito, SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Dulces Kokito, SA de CV is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for coconut bar pineapple flavor; coconut bar candy white; FDA published the listing on January 24, 2018.
- Has FDA refused shipments from Dulces Kokito, SA de CV?
- Yes. FDA refused 5 shipment lines from Dulces Kokito, SA de CV between February 24, 2017 and April 24, 2026. The most recent, on April 24, 2026, was candy specialties, n.e.c. (without chocolate), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Dulces Kokito, SA de CV's shipments?
- The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 2 lines) and COLOR LBLG (artificial coloring not declared, 1 line).
- When was Dulces Kokito, SA de CV last inspected by FDA?
- FDA's most recent inspection of Dulces Kokito, SA de CV with a final classification is dated June 23, 2023 and was classified VAI (Voluntary Action Indicated).
- What is Dulces Kokito, SA de CV's FEI number?
- Dulces Kokito, SA de CV's FDA Establishment Identifier (FEI) is 3004971614.
- Can shipments from Dulces Kokito, SA de CV still enter the U.S.?
- Shipments of coconut bar pineapple flavor; coconut bar candy white from Dulces Kokito, SA de CV can be detained without physical examination under Import Alert 99-21; 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).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.