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Holle Europe GmbH

FDA import alert and refusal historyLorrach, GermanyFEI 3046304548

Recorded by FDA as HOLLE EUROPE GMBH

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Example subjectHolle Europe Gmb added to Import Alert 16-129 (red list)

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As of October 26, 2026, Holle Europe GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 2, 2026, most often for false or misleading labeling (FALSE).

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

Current status

Import alerts
Not listed
Last import refusal
Goat milk infant based formula product (0-12 months), powder formula · LIST INGRE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Holle Europe GmbH

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

2026

  1. Import refusal
    Refused, Goat milk infant based formula product (0-12 months), powder formulaLIST INGREFALSELACKS N/CEntry 1FX-6002544-2
    Source

Refusal charges, in plain English

  • FALSE1 refused line

    False or misleading labeling

    The labeling appeared to be false or misleading in some particular.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

  • LIST INGRE1 refused line

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

Questions about Holle Europe GmbH

Is Holle Europe GmbH on an FDA import alert?
No listing for Holle Europe GmbH appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
Has FDA refused shipments from Holle Europe GmbH?
Yes. FDA refused 1 shipment line from Holle Europe GmbH on October 2, 2026. The most recent, on October 2, 2026, was goat milk infant based formula product (0-12 months), powder formula, charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Holle Europe GmbH's shipments?
The most frequent charges are FALSE (false or misleading labeling, 1 line) and LACKS N/C (net quantity statement missing, 1 line).
What is Holle Europe GmbH's FEI number?
Holle Europe GmbH's FDA Establishment Identifier (FEI) is 3046304548.

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Example subjectHolle Europe Gmb 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.