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Nestle Trinidad and Tobago

FDA import alert and refusal historyPort-of-Spain, Trinidad and TobagoFEI 3013364680

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Example subjectNestle Trinidad and Tobag added to Import Alert 16-129 (red list)

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As of October 26, 2026, Nestle Trinidad and Tobago (Port-of-Spain, Trinidad and Tobago) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for sorrel drink; orchard fruit punch, published by FDA on May 13, 2016, and has 5 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Soft drinks and waters not mentioned elsewhere, n.e.c. · LACKS N/C
Last warning letter
None found
Last inspection
None on record

Every FDA record for Nestle Trinidad and Tobago

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

2022

  1. Import refusal
    Refused, 2 lines in one entry: Soft drinks and waters not mentioned elsewhere, n.e.c.LACKS N/CNUTRIT LBLNEEDS FCENO PROCESSEntry EUX-0131763-5Show 2 lines
    Source

2017

  1. Import refusal
    Refused, 3 lines in one entry: Soft drink, subtropical or tropical fruit flavored, noncarbonated; Noncarbonated soft drink, n.e.c. and 1 moreLABELINGNUTRIT LBLEntry 101-5268947-7Show 3 lines
    Source

2016

  1. Import alert listing
    Listed on Import Alert 45-02red listSorrel Drink; Orchard Fruit Punch
    Source

Refusal charges, in plain English

  • 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.

  • LABELING3 refused lines

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • 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.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

Questions about Nestle Trinidad and Tobago

Is Nestle Trinidad and Tobago on an FDA import alert?
Yes. As of October 26, 2026, Nestle Trinidad and Tobago is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for sorrel drink; orchard fruit punch; FDA published the listing on May 13, 2016.
Has FDA refused shipments from Nestle Trinidad and Tobago?
Yes. FDA refused 5 shipment lines from Nestle Trinidad and Tobago between February 17, 2017 and September 16, 2022. The most recent, on September 16, 2022, was soft drinks and waters not mentioned elsewhere, n.e.c., charged as LACKS N/C (net quantity statement missing).
Why did FDA refuse Nestle Trinidad and Tobago's shipments?
The most frequent charges are NUTRIT LBL (nutrition information missing from label, 4 lines) and LABELING (fair packaging and labeling act, 3 lines).
What is Nestle Trinidad and Tobago's FEI number?
Nestle Trinidad and Tobago's FDA Establishment Identifier (FEI) is 3013364680.
Can shipments from Nestle Trinidad and Tobago still enter the U.S.?
Shipments of sorrel drink; orchard fruit punch from Nestle Trinidad and Tobago 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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Example subjectNestle Trinidad and Tobag added to Import Alert 16-129 (red list)

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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.