Is Karafi Limited on an FDA import alert?

No listing for Karafi Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Ghana page.

Has FDA refused shipments from Karafi Limited?

Yes. FDA refused 4 shipment lines from Karafi Limited between June 1, 2020 and January 14, 2026. The most recent, on January 14, 2026, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).

Why did FDA refuse Karafi Limited's shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 4 lines) and DIRECTIONS (directions, 1 line).

What is Karafi Limited's FEI number?

Karafi Limited's FDA Establishment Identifier (FEI) is 3011424182.

Karafi Limited

FDA import alert and refusal historyTakoradi, GhanaFEI 3011424182

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As of October 26, 2026, Karafi Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between June 1, 2020 and January 14, 2026, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Jan 14, 2026Herbals & botanicals (not teas), n.e.c. · UNAPPROVED
Last warning letter: None found
Last inspection: None on record

Every FDA record for Karafi Limited

4 records, newest first. Each line links to the FDA page it came from.

2026

Jan 14, 2026Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry N56-0050650-9
Source

2024

May 28, 2024Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry BNI-0125245-9
Source
Jan 23, 2024Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry 8B4-0005486-0
Source

2020

Jun 1, 2020Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.DIRECTIONS UNAPPROVEDEntry W04-0072004-5
Source

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.
DIRECTIONS1 refused line
DIRECTIONS

Questions about Karafi Limited

Is Karafi Limited on an FDA import alert?: No listing for Karafi Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Ghana page.
Has FDA refused shipments from Karafi Limited?: Yes. FDA refused 4 shipment lines from Karafi Limited between June 1, 2020 and January 14, 2026. The most recent, on January 14, 2026, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Karafi Limited's shipments?: The most frequent charges are UNAPPROVED (unapproved new drug, 4 lines) and DIRECTIONS (directions, 1 line).
What is Karafi Limited's FEI number?: Karafi Limited's FDA Establishment Identifier (FEI) is 3011424182.

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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.