Horphag Research (Europe) Ltd
FDA import alert and refusal historyLemesos, CyprusFEI 3010275290
As of October 26, 2026, Horphag Research (Europe) Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between December 7, 2017 and July 21, 2021, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, n.e.c. · DIRSEXMPT
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Horphag Research (Europe) Ltd
4 records, newest first. Each line links to the FDA page it came from.
2021
- Import refusalRefused, Vitamin, n.e.c.DIRSEXMPTUNAPPROVEDEntry NEN-0003277-0Source
2018
- Import refusalRefused, Vitamin, n.e.c.UNAPPROVEDEntry FT9-3005984-3Source
- Import refusalRefused, Vitamin, n.e.c.UNAPPROVEDEntry FT9-3005277-2Source
2017
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNSAFE COLDIRECTIONSCOLOR LBLGNUTRIT LBLUNAPPROVEDEntry FT9-3004008-2Source
Refusal charges, in plain English
- UNAPPROVED4 refused lines
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- DIRECTIONS1 refused line
DIRECTIONS
- DIRSEXMPT1 refused line
DIRSEXMPT
- 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.
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Horphag Research (Europe) Ltd
- Is Horphag Research (Europe) Ltd on an FDA import alert?
- No listing for Horphag Research (Europe) Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Cyprus page.
- Has FDA refused shipments from Horphag Research (Europe) Ltd?
- Yes. FDA refused 4 shipment lines from Horphag Research (Europe) Ltd between December 7, 2017 and July 21, 2021. The most recent, on July 21, 2021, was vitamin, n.e.c., charged as DIRSEXMPT (dirsexmpt).
- Why did FDA refuse Horphag Research (Europe) Ltd's shipments?
- The most frequent charges are UNAPPROVED (unapproved new drug, 4 lines) and COLOR LBLG (artificial coloring not declared, 1 line).
- What is Horphag Research (Europe) Ltd's FEI number?
- Horphag Research (Europe) Ltd's FDA Establishment Identifier (FEI) is 3010275290.
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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.