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Uplove Global Ventures

FDA import alert and refusal historyIganmu, NigeriaFEI 3017958379

Recorded by FDA as UPLOVE GLOBAL VENTURES

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Example subjectUplove Global Venture added to Import Alert 16-129 (red list)

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As of October 26, 2026, Uplove Global Ventures is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 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, dried or paste · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Uplove Global Ventures

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

2023

  1. Import refusal
    Refused, Tamarind, dried or pasteFILTHYEntry 9RN-1209789-2
    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 Uplove Global Ventures

Is Uplove Global Ventures on an FDA import alert?
No listing for Uplove Global Ventures appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Nigeria page.
Has FDA refused shipments from Uplove Global Ventures?
Yes. FDA refused 1 shipment line from Uplove Global Ventures on January 11, 2023. The most recent, on January 11, 2023, was tamarind, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Uplove Global Ventures's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Uplove Global Ventures's FEI number?
Uplove Global Ventures's FDA Establishment Identifier (FEI) is 3017958379.

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Example subjectUplove Global Venture 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.