Chocolate Mayordomo de Oaxaca
FDA import alert and refusal historyOaxaca, MexicoFEI 3003549656
As of October 26, 2026, Chocolate Mayordomo de Oaxaca (Oaxaca, Mexico) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for mole paste red (mole rojo), published by FDA on May 3, 2018, and has 6 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- Mole paste · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Chocolate Mayordomo de Oaxaca
7 records, newest first. Each line links to the FDA page it came from.
2021
- Import refusalRefused, Mole pasteLIST INGREINCONSPICUEntry EEE-0073556-2Source
2020
- Import refusalRefused, Mole pasteFALSENO ENGLISHUSUAL NAMENUTRIT LBLEntry 9UG-0086671-1Source
- Import refusalRefused, Mole pasteNUTRIT LBLEntry 89G-0002999-7Source
2018
- Import refusalRefused, Mole pasteLIST INGREINCONSPICUPRESRV LBLALLERGENNUTRIT LBLEntry APF-0023205-6Source
- Import refusalRefused, Mole pasteLIST INGRENO ENGLISHNUTRIT LBLEntry WC1-6801632-5Source
- Import alert listingListed on Import Alert 99-39red listMole Paste Red (Mole Rojo)Source
- Import refusalRefused, Mole pasteLIST INGREINCONSPICUNEEDS FCEEntry APF-0021900-4Source
Refusal charges, in plain English
- LIST INGRE4 refused lines
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 LBL4 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- INCONSPICU3 refused lines
Required information not conspicuous
Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.
- NO ENGLISH2 refused lines
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.
- 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.
- NEEDS FCE1 refused line
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
- PRESRV LBL1 refused line
Chemical preservative not declared
The product appeared to contain a chemical preservative without labeling that states that fact and the preservative's function.
Questions about Chocolate Mayordomo de Oaxaca
- Is Chocolate Mayordomo de Oaxaca on an FDA import alert?
- Yes. As of October 26, 2026, Chocolate Mayordomo de Oaxaca is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for mole paste red (mole rojo); FDA published the listing on May 3, 2018.
- Has FDA refused shipments from Chocolate Mayordomo de Oaxaca?
- Yes. FDA refused 6 shipment lines from Chocolate Mayordomo de Oaxaca between February 14, 2018 and February 25, 2021. The most recent, on February 25, 2021, was mole paste, charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Chocolate Mayordomo de Oaxaca's shipments?
- The most frequent charges are LIST INGRE (ingredients not listed, 4 lines) and NUTRIT LBL (nutrition information missing from label, 4 lines).
- What is Chocolate Mayordomo de Oaxaca's FEI number?
- Chocolate Mayordomo de Oaxaca's FDA Establishment Identifier (FEI) is 3003549656.
- Can shipments from Chocolate Mayordomo de Oaxaca still enter the U.S.?
- Shipments of mole paste red (mole rojo) from Chocolate Mayordomo de Oaxaca can be detained without physical examination under Import Alert 99-39; 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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