OSWALD MARTIN
⚠️ Moderate Risk
FEI: 3012491993 • TRELAWNY • JAMAICA
FEI Number
3012491993
Location
TRELAWNY
Country
JAMAICAAddress
CARREY PARK DUNCANS P.O, , TRELAWNY, , Jamaica
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/26/2024 | 25JFC37YAMS (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Division of Southeast Imports (DSEI) |
| 6/28/2023 | 25JFC37YAMS (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Division of Southeast Imports (DSEI) |
| 12/5/2022 | 25JFC23TARO, DASHEEN (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Division of Northeast Imports (DNEI) |
| 9/8/2021 | 07YYY99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C. | 249FILTHY | Division of Northeast Imports (DNEI) |
| 1/11/2010 | 24FGB05PUMPKINS (FRUIT USED AS VEGETABLE) | Division of Northeast Imports (DNEI) | |
| 1/11/2010 | 24TGC45SUGAR CANE (LEAF & STEM VEGETABLE) | Division of Northeast Imports (DNEI) | |
| 1/11/2010 | 21SFC09BREADFRUIT (SUBTROPICAL AND TROPICAL FRUIT) | Division of Northeast Imports (DNEI) | |
| 11/26/2008 | 24TEE99LEAF & STEM VEGETABLES, N.E.C. | 251POISONOUS | New York District Office (NYK-DO) |
Frequently Asked Questions
What is OSWALD MARTIN's FDA import refusal history?
OSWALD MARTIN (FEI: 3012491993) has 8 FDA import refusal record(s) in our database, spanning from 11/26/2008 to 8/26/2024.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. OSWALD MARTIN's FEI number is 3012491993.
What types of violations has OSWALD MARTIN received?
OSWALD MARTIN has been cited for 5 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about OSWALD MARTIN come from?
All FDA import refusal data for OSWALD MARTIN is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.