ALTERA PUBLICIDAD SA de CV
FDA import alert and refusal historyCajeme, MexicoFEI 3013008492
As of October 26, 2026, ALTERA PUBLICIDAD SA de CV (Cajeme, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for chamoy sauce, published by FDA on December 18, 2015, and has 7 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 without chocolate n.e.c. · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for ALTERA PUBLICIDAD SA de CV
8 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Candy without chocolate n.e.c.UNSAFE COLCOLOR LBLGEntry 92Q-0028084-1Source
2018
- Import refusalSource
Refused, 2 lines in one entry: Standardized mixed nut productPRESRV LBLEntry 92Q-0007511-8Show 2 linesHide lines
- Refused, Standardized mixed nut productPRESRV LBLEntry 92Q-0007511-8Source
- Refused, Standardized mixed nut productPRESRV LBLEntry 92Q-0007511-8Source
- Import refusalSource
Refused, 4 lines in one entry: Pepper sauce (hot, mild, etc.)NEEDS FCENO PROCESSEntry 92Q-0006271-0Show 4 linesHide lines
- Refused, Pepper sauce (hot, mild, etc.)NEEDS FCENO PROCESSEntry 92Q-0006271-0Source
- Refused, Pepper sauce (hot, mild, etc.)NEEDS FCENO PROCESSEntry 92Q-0006271-0Source
- Refused, Pepper sauce (hot, mild, etc.)NEEDS FCENO PROCESSEntry 92Q-0006271-0Source
- Refused, Pepper sauce (hot, mild, etc.)NEEDS FCENO PROCESSEntry 92Q-0006271-0Source
2015
- Import alert listingListed on Import Alert 45-02red listChamoy sauceSource
Refusal charges, in plain English
- NEEDS FCE4 refused lines
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.
- NO PROCESS4 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
- PRESRV LBL2 refused lines
Chemical preservative not declared
The product appeared to contain a chemical preservative without labeling that states that fact and the preservative's function.
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- 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 ALTERA PUBLICIDAD SA de CV
- Is ALTERA PUBLICIDAD SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, ALTERA PUBLICIDAD SA de CV is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for chamoy sauce; FDA published the listing on December 18, 2015.
- Has FDA refused shipments from ALTERA PUBLICIDAD SA de CV?
- Yes. FDA refused 7 shipment lines from ALTERA PUBLICIDAD SA de CV between April 5, 2018 and June 13, 2025. The most recent, on June 13, 2025, was candy without chocolate n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse ALTERA PUBLICIDAD SA de CV's shipments?
- The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 4 lines) and NO PROCESS (no scheduled process filed, 4 lines).
- What is ALTERA PUBLICIDAD SA de CV's FEI number?
- ALTERA PUBLICIDAD SA de CV's FDA Establishment Identifier (FEI) is 3013008492.
- Can shipments from ALTERA PUBLICIDAD SA de CV still enter the U.S.?
- Shipments of chamoy sauce from ALTERA PUBLICIDAD 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).
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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.