Friesenkrone Feinkost
FDA import alert and refusal historyMarne, GermanyFEI 3003481713
As of October 26, 2026, Friesenkrone Feinkost (Marne, Germany) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for herring, published by FDA on March 13, 2009, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-39 · red list
- Last import refusal
- Herring · LISTERIA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Friesenkrone Feinkost
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- LISTERIA2 refused lines
Listeria monocytogenes
The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Friesenkrone Feinkost
- Is Friesenkrone Feinkost on an FDA import alert?
- Yes. As of October 26, 2026, Friesenkrone Feinkost is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for herring; FDA published the listing on March 13, 2009.
- Has FDA refused shipments from Friesenkrone Feinkost?
- Yes. FDA refused 2 shipment lines from Friesenkrone Feinkost between April 3, 2019 and January 6, 2021. The most recent, on January 6, 2021, was herring, charged as LISTERIA (listeria monocytogenes).
- Why did FDA refuse Friesenkrone Feinkost's shipments?
- The most frequent charge is LISTERIA (listeria monocytogenes, 2 lines).
- What is Friesenkrone Feinkost's FEI number?
- Friesenkrone Feinkost's FDA Establishment Identifier (FEI) is 3003481713.
- Can shipments from Friesenkrone Feinkost still enter the U.S.?
- Shipments of herring from Friesenkrone Feinkost can be detained without physical examination under Import Alert 16-39; 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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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.