Lofotfisk A.S.
FDA import alert and refusal historyB?stad, NorwayFEI 1000152936
As of October 25, 2026, Lofotfisk A.S. (B?stad, Norway) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for salmon (humpback, silver, king sockeye, etc.), hot smoked, fish; salmon (humpback, silver, king, sockeye, etc.), cold smoked, fish; smoked salmon, published by FDA on March 13, 2009, and has no 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
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Lofotfisk A.S.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-39red listSalmon (Humpback, Silver, King Sockeye, etc.), Hot Smoked, Fish; Salmon (Humpback, Silver, King, Sockeye, etc.), Cold Smoked, Fish; Smoked salmonSource
Questions about Lofotfisk A.S.
- Is Lofotfisk A.S. on an FDA import alert?
- Yes. As of October 25, 2026, Lofotfisk A.S. is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for salmon (humpback, silver, king sockeye, etc.), hot smoked, fish; salmon (humpback, silver, king, sockeye, etc.), cold smoked, fish; smoked salmon; FDA published the listing on March 13, 2009.
- Has FDA refused shipments from Lofotfisk A.S.?
- No FDA import refusals for Lofotfisk A.S. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Lofotfisk A.S.'s FEI number?
- Lofotfisk A.S.'s FDA Establishment Identifier (FEI) is 1000152936.
- Can shipments from Lofotfisk A.S. still enter the U.S.?
- Shipments of salmon (humpback, silver, king sockeye, etc.), hot smoked, fish; salmon (humpback, silver, king, sockeye, etc.), cold smoked, fish; smoked salmon from Lofotfisk A.S. 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.