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Frezco Beverages

FDA import alert and refusal historyNadi, FijiFEI 3007829284

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Example subjectFrezco Beverage added to Import Alert 16-129 (red list)

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As of October 25, 2026, Frezco Beverages (Nadi, Fiji) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for noni juice, published by FDA on November 4, 2022, is also listed on Import Alert 54-14 (red list) and Import Alert 45-02 (red list), and has 9 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Soft drink, cola, carbonated · UNSAFE COL
Last warning letter
None found
Last inspection
Classified OAI (Official Action Indicated)

Every FDA record for Frezco Beverages

13 records, newest first. Each line links to the FDA page it came from.

2022

  1. Import alert listing
    Listed on Import Alert 99-39red listNoni juice
    Source
  2. Import alert listing
    Listed on Import Alert 54-14red listNoni juice
    Source
  3. Inspection
    Inspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source
  4. Import refusal
    Refused, 5 lines in one entry: Soft drink, cola, carbonated; Soft drink, citrus fruit flavored, carbonated and 2 moreUNSAFE COLCOLOR LBLGEntry E6G-0171533-8Show 5 lines
    Source

2020

  1. Import refusal
    Refused, 4 lines in one entry: Noni (herbal & botanicals, not teas); Soft drink, berry fruit flavored, carbonated and 1 moreNEEDS FCENO PROCESSUNSAFE COLCOLOR LBLGEntry 9GW-0009086-0Show 4 lines
    Source

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listPineapple flavor drink; Pops Fruit Cocktail Flavor Drink; raspberry soda; orange soda; lime soda; kola pops soft drink; raspberry cordial
    Source

Refusal charges, in plain English

  • COLOR LBLG7 refused lines

    Artificial coloring not declared

    The product appeared to contain an artificial coloring without labeling that states that fact.

  • UNSAFE COL7 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.

  • NEEDS FCE2 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 PROCESS2 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.

Questions about Frezco Beverages

Is Frezco Beverages on an FDA import alert?
Yes. As of October 25, 2026, Frezco Beverages is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for noni juice; FDA published the listing on November 4, 2022.
Has FDA refused shipments from Frezco Beverages?
Yes. FDA refused 9 shipment lines from Frezco Beverages between June 10, 2020 and February 17, 2022. The most recent, on February 17, 2022, was soft drink, cola, carbonated, charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Frezco Beverages's shipments?
The most frequent charges are COLOR LBLG (artificial coloring not declared, 7 lines) and UNSAFE COL (color additive unsafe under section 721, 7 lines).
When was Frezco Beverages last inspected by FDA?
FDA's most recent inspection of Frezco Beverages with a final classification is dated March 23, 2022 and was classified OAI (Official Action Indicated).
What is Frezco Beverages's FEI number?
Frezco Beverages's FDA Establishment Identifier (FEI) is 3007829284.
Can shipments from Frezco Beverages still enter the U.S.?
Shipments of noni juice from Frezco Beverages 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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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.