Is Haribo BV on an FDA import alert?

No listing for Haribo BV 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 Haribo BV?

Yes. FDA refused 9 shipment lines from Haribo BV between March 21, 2017 and May 25, 2017. The most recent, on May 25, 2017, was flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate), charged as NO ENGLISH (required label information not in english).

Why did FDA refuse Haribo BV's shipments?

The most frequent charge is NO ENGLISH (required label information not in english, 9 lines).

What is Haribo BV's FEI number?

Haribo BV's FDA Establishment Identifier (FEI) is 3013215681.

Haribo BV

FDA import alert and refusal historyNoord Brabant, NetherlandsFEI 3013215681

Recorded by FDA as HARIBO BV

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As of October 26, 2026, Haribo BV is not on any FDA import alert in SupplierRadar's records; FDA refused 9 of its shipment lines between March 21, 2017 and May 25, 2017, most often for required label information not in english (NO ENGLISH).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: May 25, 2017Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate) · NO ENGLISH
Last warning letter: None found
Last inspection: None on record

Every FDA record for Haribo BV

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

2017

May 25, 2017Import refusal
Refused, 7 lines in one entry: Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3455911-9Show 7 linesHide lines
- Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3455911-9Source
- Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3455911-9Source
- Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3455911-9Source
- Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3455911-9Source
- Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3455911-9Source
- Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3455911-9Source
- Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3455911-9Source
Source
Mar 22, 2017Import refusal
Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3022625-9
Source
Mar 21, 2017Import refusal
Refused, Flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate)NO ENGLISHEntry AEK-3032614-1
Source

Refusal charges, in plain English

NO ENGLISH9 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 Haribo BV

Is Haribo BV on an FDA import alert?: No listing for Haribo BV 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 Haribo BV?: Yes. FDA refused 9 shipment lines from Haribo BV between March 21, 2017 and May 25, 2017. The most recent, on May 25, 2017, was flavored candy, soft (live savers, etc.), without nuts and fruit (without chocolate), charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Haribo BV's shipments?: The most frequent charge is NO ENGLISH (required label information not in english, 9 lines).
What is Haribo BV's FEI number?: Haribo BV's FDA Establishment Identifier (FEI) is 3013215681.

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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.