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Milo Content

FDA import alert and refusal historyLeogane, HaitiFEI 3018287015

Recorded by FDA as MILO CONTENT

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Example subjectMilo Conten added to Import Alert 16-129 (red list)

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As of October 26, 2026, Milo Content (Leogane, Haiti) is on the red list of FDA Import Alert 23-14 (Food products: mycotoxins) for peanut butter, published by FDA on June 11, 2021, and has 1 FDA import refusal recorded since October 2016.

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

Current status

Last import refusal
Peanut, butter · AFLATOXIN
Last warning letter
None found
Last inspection
None on record

Every FDA record for Milo Content

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

2021

  1. Import alert listing
    Listed on Import Alert 23-14red listPeanut Butter
    Source
  2. Import refusal
    Refused, Peanut, butterAFLATOXINEntry FL2-0064326-8
    Source

Refusal charges, in plain English

Questions about Milo Content

Is Milo Content on an FDA import alert?
Yes. As of October 26, 2026, Milo Content is on the red list of FDA Import Alert 23-14, “Food products: mycotoxins”, for peanut butter; FDA published the listing on June 11, 2021.
Has FDA refused shipments from Milo Content?
Yes. FDA refused 1 shipment line from Milo Content on May 28, 2021. The most recent, on May 28, 2021, was peanut, butter, charged as AFLATOXIN (aflatoxin).
Why did FDA refuse Milo Content's shipments?
The most frequent charge is AFLATOXIN (aflatoxin, 1 line).
What is Milo Content's FEI number?
Milo Content's FDA Establishment Identifier (FEI) is 3018287015.
Can shipments from Milo Content still enter the U.S.?
Shipments of peanut butter from Milo Content can be detained without physical examination under Import Alert 23-14; 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 subjectMilo Conten 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.