Grace Kennedy Jamaica Ltd.
FDA import alert and refusal historyKingston, JamaicaFEI 3007477618
Recorded by FDA as GRACE KENNEDY JAMAICA LTD.
As of October 26, 2026, Grace Kennedy Jamaica Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 22, 2024, 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
- Chocolate plain cookies,biscuits and wafers · VITAMN LBL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Grace Kennedy Jamaica Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2024
- Import refusalRefused, Chocolate plain cookies,biscuits and wafersVITAMN LBLALLERGENEntry K51-0105886-2Source
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.
- VITAMN LBL1 refused line
VITAMN LBL
Questions about Grace Kennedy Jamaica Ltd.
- Is Grace Kennedy Jamaica Ltd. on an FDA import alert?
- No listing for Grace Kennedy Jamaica Ltd. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Jamaica page.
- Has FDA refused shipments from Grace Kennedy Jamaica Ltd.?
- Yes. FDA refused 1 shipment line from Grace Kennedy Jamaica Ltd. on August 22, 2024. The most recent, on August 22, 2024, was chocolate plain cookies,biscuits and wafers, charged as VITAMN LBL (vitamn lbl).
- Why did FDA refuse Grace Kennedy Jamaica Ltd.'s shipments?
- The most frequent charges are ALLERGEN (major food allergen not declared, 1 line) and VITAMN LBL (vitamn lbl, 1 line).
- What is Grace Kennedy Jamaica Ltd.'s FEI number?
- Grace Kennedy Jamaica Ltd.'s FDA Establishment Identifier (FEI) is 3007477618.
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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.