SupplierRadar

Paula'S Confectionary

FDA import alert and refusal historyDiego Martin, Trinidad and TobagoFEI 3005054561

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Example subjectPaula'S Confectionar added to Import Alert 16-129 (red list)

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As of October 26, 2026, Paula'S Confectionary is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 11, 2023, most often for filthy, putrid or decomposed substance (FILTHY).

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

Current status

Import alerts
Not listed
Last import refusal
Tamarind, topping or syrup · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Paula'S Confectionary

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

2023

  1. Import refusal
    Refused, Tamarind, topping or syrupFILTHYEntry 9UA-0289783-5
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Paula'S Confectionary

Is Paula'S Confectionary on an FDA import alert?
No listing for Paula'S Confectionary appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Trinidad and Tobago page.
Has FDA refused shipments from Paula'S Confectionary?
Yes. FDA refused 1 shipment line from Paula'S Confectionary on May 11, 2023. The most recent, on May 11, 2023, was tamarind, topping or syrup, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Paula'S Confectionary's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Paula'S Confectionary's FEI number?
Paula'S Confectionary's FDA Establishment Identifier (FEI) is 3005054561.

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Example subjectPaula'S Confectionar 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.