Ogura Shokuhin Co Ltd
FDA import alert and refusal historyShizuoka, JapanFEI 1000203650
Recorded by FDA as Ogura Shokuhin Co Ltd; Ogura Shokuhin Co. Ltd.
As of October 26, 2026, Ogura Shokuhin Co Ltd (Shizuoka, Japan) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for seasoned fish flakes, published by FDA on September 9, 2024, is also listed on Import Alert 99-22 (red list) and Import Alert 16-120 (red list) and Import Alert 99-39 (red list) and Import Alert 16-74 (red list), and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red listIA 99-22 · red listIA 16-120 · red listIA 99-39 · red listIA 16-74 · red list
- Last import refusal
- Cod · LIST INGRE
- Last warning letter
- Seafood HACCP/CGMP for Foods/Adulterated/Insanitary Conditions
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Ogura Shokuhin Co Ltd
8 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, CodLIST INGREMFRHACCPFALSEUSUAL NAMEALLERGENNUTRIT LBLEntry 235-1735799-4Source
2024
- Import alert listingListed on Import Alert 45-02red listSeasoned Fish FlakesSource
- Import alert listingListed on Import Alert 99-22red listSeasoned Alaska Pollock PowderSource
- Import alert listingListed on Import Alert 16-120red listReady-to-eat; shelf stable fish productsSource
- Import alert listingListed on Import Alert 99-39red listSeasoned Alaska Pollock Powder; Dried Sardine; Dried Prepared Sardine productsSource
- Warning letterWarning letter issuedSeafood HACCP/CGMP for Foods/Adulterated/Insanitary ConditionsSource
2019
- Import alert listingListed on Import Alert 16-74red listBoiled small anchovy taberu kozakana)Source
2009
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
- ALLERGEN1 refused line
Major food allergen not declared
The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.
- FALSE1 refused line
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
- 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).
- MFRHACCP1 refused line
Seafood HACCP requirements not met
The seafood appeared to have been processed without meeting the seafood HACCP requirements in 21 CFR 123.6(a) and 123.8(a), so it is treated as prepared under insanitary conditions.
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- USUAL NAME1 refused line
Common or usual name missing
The label appeared not to show the common or usual name of the food.
Questions about Ogura Shokuhin Co Ltd
- Is Ogura Shokuhin Co Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Ogura Shokuhin Co Ltd is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for seasoned fish flakes; FDA published the listing on September 9, 2024.
- Has FDA refused shipments from Ogura Shokuhin Co Ltd?
- Yes. FDA refused 1 shipment line from Ogura Shokuhin Co Ltd on January 22, 2025. The most recent, on January 22, 2025, was cod, charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Ogura Shokuhin Co Ltd's shipments?
- The most frequent charges are ALLERGEN (major food allergen not declared, 1 line) and FALSE (false or misleading labeling, 1 line).
- Has Ogura Shokuhin Co Ltd received an FDA warning letter?
- Yes. FDA issued a warning letter to Ogura Shokuhin Co Ltd on May 1, 2024 (Seafood HACCP/CGMP for Foods/Adulterated/Insanitary Conditions).
- When was Ogura Shokuhin Co Ltd last inspected by FDA?
- FDA's most recent inspection of Ogura Shokuhin Co Ltd with a final classification is dated November 17, 2009 and was classified OAI (Official Action Indicated).
- What is Ogura Shokuhin Co Ltd's FEI number?
- Ogura Shokuhin Co Ltd's FDA Establishment Identifier (FEI) is 1000203650.
- Can shipments from Ogura Shokuhin Co Ltd still enter the U.S.?
- Shipments of seasoned fish flakes from Ogura Shokuhin Co Ltd can be detained without physical examination under Import Alert 45-02; 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.