Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V.
FDA import alert and refusal historyCalvillo, MexicoFEI 3012691200
As of October 27, 2026, Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V. (Calvillo, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for guava jam, published by FDA on December 15, 2014, 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 45-02 · red list
- Last import refusal
- Candy specialties, n.e.c. (without chocolate) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V.
6 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Candy specialties, n.e.c. (without chocolate)FILTHYNO ENGLISHEntry DR4-0668962-7Source
2023
- Import refusalRefused, Guava, jam, jelly, preserves, marmalade, butter or candiedUNSAFE COLCOLOR LBLGNUTRIT LBLEntry DR4-0580530-7Source
2022
- Import refusalRefused, Guava, jam, jelly, preserves, marmalade, butter or candiedUNSAFE COLCOLOR LBLGEntry N9H-0006165-3Source
- Import refusalRefused, Guava, jam, jelly, preserves, marmalade, butter or candiedUNSAFE COLCOLOR LBLGEntry N9H-0006007-7Source
2020
- Import refusalRefused, Guava, jam, jelly, preserves, marmalade, butter or candiedUNSAFE COLCOLOR LBLGEntry DR4-0414173-8Source
2014
- Import alert listingListed on Import Alert 45-02red listGuava JamSource
Refusal charges, in plain English
- COLOR LBLG4 refused lines
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- UNSAFE COL4 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.
- 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.
- NO ENGLISH1 refused line
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
- 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 Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V.
- Is Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V. on an FDA import alert?
- Yes. As of October 27, 2026, Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for guava jam; FDA published the listing on December 15, 2014.
- Has FDA refused shipments from Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V.?
- Yes. FDA refused 5 shipment lines from Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V. between October 21, 2020 and November 12, 2025. The most recent, on November 12, 2025, was candy specialties, n.e.c. (without chocolate), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V.'s shipments?
- The most frequent charges are COLOR LBLG (artificial coloring not declared, 4 lines) and UNSAFE COL (color additive unsafe under section 721, 4 lines).
- What is Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V.'s FEI number?
- Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V.'s FDA Establishment Identifier (FEI) is 3012691200.
- Can shipments from Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V. still enter the U.S.?
- Shipments of guava jam from Fabrica de Dulces Flor de Calvillo, S. de R.L. M.I. de C.V. can be detained without physical examination under Import Alert 45-02; 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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