Postobon
FDA import alert and refusal historyMedellin, ColombiaFEI 3010888137
As of October 25, 2026, Postobon is not on any FDA import alert in SupplierRadar's records; FDA refused 9 of its shipment lines between November 26, 2019 and August 4, 2026, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Fruit beverage bases, liquid, n.e.c. · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Postobon
9 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalSource
Refused, 3 lines in one entry: Fruit beverage bases, liquid, n.e.c.NO ENGLISHUSUAL NAMENUTRIT LBLEntry EQW-0060917-4Show 3 linesHide lines
- Refused, Fruit beverage bases, liquid, n.e.c.NO ENGLISHUSUAL NAMENUTRIT LBLEntry EQW-0060917-4Source
- Refused, Fruit beverage bases, liquid, n.e.c.NO ENGLISHUSUAL NAMENUTRIT LBLEntry EQW-0060917-4Source
- Refused, Fruit beverage bases, liquid, n.e.c.NO ENGLISHUSUAL NAMENUTRIT LBLEntry EQW-0060917-4Source
2024
- Import refusalSource
Refused, 2 lines in one entry: Soft drink, berry fruit flavored, carbonatedUNSAFE COLNO ENGLISHEntry AMN-0093368-5Show 2 linesHide lines
- Refused, Soft drink, berry fruit flavored, carbonatedUNSAFE COLEntry AMN-0093368-5Source
- Refused, Soft drink, berry fruit flavored, carbonatedNO ENGLISHEntry AMN-0093368-5Source
2022
- Import refusalRefused, Blackberry juice, berry juice or concentratesUNSAFE COLEntry AMN-0076406-4Source
- Import refusalRefused, Blackberry juice, berry juice or concentratesUNSAFE COLEntry AMN-0075060-0Source
- Import refusalRefused, Soft drink, berry fruit flavored, carbonatedCOLORLABELEntry AMN-0068577-2Source
2019
- Import refusalRefused, Nonalcoholic beverages, n.e.c.UNSAFE COLLIST INGRECOLOR LBLGEntry N56-0026565-0Source
Refusal charges, in plain English
- NO ENGLISH4 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.
- 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.
- NUTRIT LBL3 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.
- USUAL NAME3 refused lines
Common or usual name missing
The label appeared not to show the common or usual name of the food.
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- COLORLABEL1 refused line
Required information not prominent
Information required on the label appeared not to be placed prominently enough, or in such terms, to be read and understood by an ordinary consumer.
- 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).
Questions about Postobon
- Is Postobon on an FDA import alert?
- No listing for Postobon appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Colombia page.
- Has FDA refused shipments from Postobon?
- Yes. FDA refused 9 shipment lines from Postobon between November 26, 2019 and August 4, 2026. The most recent, on August 4, 2026, was fruit beverage bases, liquid, n.e.c., charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Postobon's shipments?
- The most frequent charges are NO ENGLISH (required label information not in english, 4 lines) and UNSAFE COL (color additive unsafe under section 721, 4 lines).
- What is Postobon's FEI number?
- Postobon's FDA Establishment Identifier (FEI) is 3010888137.
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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.