Unilever BV
FDA import alert and refusal historyRotterdam, NetherlandsFEI 3013231171
Recorded by FDA as UNILEVER BV
As of October 25, 2026, Unilever BV is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between March 21, 2017 and March 22, 2017, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Mixed spices and seasoning with salt, n.e.c. · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Unilever BV
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Mixed spices and seasoning with salt, n.e.c.NO ENGLISHEntry AEK-3022625-9Source
- Import refusalRefused, Mixed spices and seasoning with salt, n.e.c.NO ENGLISHEntry AEK-3032614-1Source
Refusal charges, in plain English
- NO ENGLISH2 refused lines
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.
Questions about Unilever BV
- Is Unilever BV on an FDA import alert?
- No listing for Unilever BV appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
- Has FDA refused shipments from Unilever BV?
- Yes. FDA refused 2 shipment lines from Unilever BV between March 21, 2017 and March 22, 2017. The most recent, on March 22, 2017, was mixed spices and seasoning with salt, n.e.c., charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Unilever BV's shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 2 lines).
- What is Unilever BV's FEI number?
- Unilever BV's FDA Establishment Identifier (FEI) is 3013231171.
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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.