Biokor
FDA import alert and refusal historyPenza, RussiaFEI 3008315374
As of October 26, 2026, Biokor is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on December 18, 2017, most often for major food allergen not declared (ALLERGEN).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Herbals & botanicals (not teas), n.e.c. · DIRECTIONS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Biokor
3 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalSource
Refused, 3 lines in one entry: Herbals & botanicals (not teas), n.e.c.DIRECTIONSLIST INGREDIETARYLBLCOLOR LBLGEntry BON-1009349-0Show 3 linesHide lines
- Refused, Herbals & botanicals (not teas), n.e.c.DIRECTIONSLIST INGREDIETARYLBLCOLOR LBLGLACKS FIRMNO ENGLISHALLERGENPLANT PARTNCONTACTEntry BON-1009349-0Source
- Refused, Herbals & botanicals (not teas), n.e.c.DIRECTIONSLIST INGREDIETARYLBLCOLOR LBLGLACKS FIRMNO ENGLISHALLERGENPLANT PARTNCONTACTEntry BON-1009349-0Source
- Refused, Herbals & botanicals (not teas), n.e.c.DIRECTIONSLIST INGREDIETARYLBLCOLOR LBLGLACKS FIRMNO ENGLISHALLERGENPLANT PARTNCONTACTEntry BON-1009349-0Source
Refusal charges, in plain English
- ALLERGEN3 refused lines
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.
- COLOR LBLG3 refused lines
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- DIETARYLBL3 refused lines
Not identified as a dietary supplement
The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).
- DIRECTIONS3 refused lines
DIRECTIONS
- LACKS FIRM3 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LIST INGRE3 refused lines
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).
- NCONTACT3 refused lines
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
- NO ENGLISH3 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 Biokor
- Is Biokor on an FDA import alert?
- No listing for Biokor appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Russia page.
- Has FDA refused shipments from Biokor?
- Yes. FDA refused 3 shipment lines from Biokor on December 18, 2017. The most recent, on December 18, 2017, was herbals & botanicals (not teas), n.e.c., charged as DIRECTIONS (directions).
- Why did FDA refuse Biokor's shipments?
- The most frequent charges are ALLERGEN (major food allergen not declared, 3 lines) and COLOR LBLG (artificial coloring not declared, 3 lines).
- What is Biokor's FEI number?
- Biokor's FDA Establishment Identifier (FEI) is 3008315374.
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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.