Cobasa Comercializadora Axiv SA de CV
FDA import alert and refusal historyGuadalajara, MexicoFEI 3010168850
Recorded by FDA as COBASA COMERCIALIZADORA AXIV SA DE CV
As of October 26, 2026, Cobasa Comercializadora Axiv SA de CV (Guadalajara, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for sprinkle style candy pieces (gragea or grajea), published by FDA on April 18, 2018, is also listed on Import Alert 99-19 (red list), and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red listIA 99-19 · red list
- Last import refusal
- Candy bar or pieces (not caramel or fondant), hard, with coconut (without chocolate) · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Cobasa Comercializadora Axiv SA de CV
4 records, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 45-02red listSprinkle Style Candy Pieces (Gragea or Grajea)Source
- Import refusalRefused, Candy bar or pieces (not caramel or fondant), hard, with coconut (without chocolate)UNSAFE COLLIST INGRECOLOR LBLGEntry DV1-0191573-9Source
2017
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2012
- Import alert listingListed on Import Alert 99-19red listOreganoSource
Refusal charges, in plain English
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- 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).
- UNSAFE COL1 refused line
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.
Questions about Cobasa Comercializadora Axiv SA de CV
- Is Cobasa Comercializadora Axiv SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Cobasa Comercializadora Axiv SA de CV is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for sprinkle style candy pieces (gragea or grajea); FDA published the listing on April 18, 2018.
- Has FDA refused shipments from Cobasa Comercializadora Axiv SA de CV?
- Yes. FDA refused 1 shipment line from Cobasa Comercializadora Axiv SA de CV on March 14, 2018. The most recent, on March 14, 2018, was candy bar or pieces (not caramel or fondant), hard, with coconut (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Cobasa Comercializadora Axiv SA de CV's shipments?
- The most frequent charges are COLOR LBLG (artificial coloring not declared, 1 line) and LIST INGRE (ingredients not listed, 1 line).
- When was Cobasa Comercializadora Axiv SA de CV last inspected by FDA?
- FDA's most recent inspection of Cobasa Comercializadora Axiv SA de CV with a final classification is dated September 22, 2017 and was classified NAI (No Action Indicated).
- What is Cobasa Comercializadora Axiv SA de CV's FEI number?
- Cobasa Comercializadora Axiv SA de CV's FDA Establishment Identifier (FEI) is 3010168850.
- Can shipments from Cobasa Comercializadora Axiv SA de CV still enter the U.S.?
- Shipments of sprinkle style candy pieces (gragea or grajea) from Cobasa Comercializadora Axiv SA de CV 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).
Buying from Cobasa Comercializadora Axiv SA de CV?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.