Unilever Benelux
FDA import alert and refusal historyRotterdam, NetherlandsFEI 3010131294
As of October 26, 2026, Unilever Benelux is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between May 25, 2017 and April 13, 2020, most often for processor not registered for canned or acidified foods (NEEDS FCE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Sauces, n.e.c. · NEEDS FCE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Unilever Benelux
2 records, newest first. Each line links to the FDA page it came from.
2020
- Import refusalRefused, Sauces, n.e.c.NEEDS FCENO PROCESSEntry W24-0363600-4Source
2017
- Import refusalRefused, Soy sauceNO ENGLISHEntry AEK-3455911-9Source
Refusal charges, in plain English
- NEEDS FCE1 refused line
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 ENGLISH1 refused line
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
- NO PROCESS1 refused line
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.
Questions about Unilever Benelux
- Is Unilever Benelux on an FDA import alert?
- No listing for Unilever Benelux appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
- Has FDA refused shipments from Unilever Benelux?
- Yes. FDA refused 2 shipment lines from Unilever Benelux between May 25, 2017 and April 13, 2020. The most recent, on April 13, 2020, was sauces, n.e.c., charged as NEEDS FCE (processor not registered for canned or acidified foods).
- Why did FDA refuse Unilever Benelux's shipments?
- The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 1 line) and NO ENGLISH (required label information not in english, 1 line).
- What is Unilever Benelux's FEI number?
- Unilever Benelux's FDA Establishment Identifier (FEI) is 3010131294.
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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.