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Coldfield Manufacturing Limited

FDA import alert and refusal historyKingston, JamaicaFEI 3004792881

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Example subjectColdfield Manufacturing Limite added to Import Alert 16-129 (red list)

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As of October 26, 2026, Coldfield Manufacturing Limited (Kingston, Jamaica) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for fruit punch drink; orange strawberry banana drink; cherry pineapple drink, published by FDA on May 27, 2011, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Coldfield Manufacturing Limited

1 record, newest first. Each line links to the FDA page it came from.

2011

  1. Import alert listing
    Listed on Import Alert 45-02red listFruit Punch Drink; Orange Strawberry Banana Drink; Cherry Pineapple Drink
    Source

Questions about Coldfield Manufacturing Limited

Is Coldfield Manufacturing Limited on an FDA import alert?
Yes. As of October 26, 2026, Coldfield Manufacturing Limited is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for fruit punch drink; orange strawberry banana drink; cherry pineapple drink; FDA published the listing on May 27, 2011.
Has FDA refused shipments from Coldfield Manufacturing Limited?
No FDA import refusals for Coldfield Manufacturing Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Coldfield Manufacturing Limited's FEI number?
Coldfield Manufacturing Limited's FDA Establishment Identifier (FEI) is 3004792881.
Can shipments from Coldfield Manufacturing Limited still enter the U.S.?
Shipments of fruit punch drink; orange strawberry banana drink; cherry pineapple drink from Coldfield Manufacturing Limited 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 subjectColdfield Manufacturing Limite 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.