PLG EXPORT IMPORT
⚠️ Moderate Risk
FEI: 3012753870 • Hagley Park, Saint Andrew • JAMAICA
FEI Number
3012753870
Location
Hagley Park, Saint Andrew
Country
JAMAICAAddress
188 Spanish Town Road, , Hagley Park, Saint Andrew, 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
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
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 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.
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
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.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/7/2016 | 21XET13ACKEES (SUBTROPICAL/TROPICAL FRUIT PULP) | 306INSANITARY | Division of Northeast Imports (DNEI) |
| 4/26/2013 | 66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C. | Division of Northeast Imports (DNEI) | |
| 3/29/2012 | 25JFC12SWEET POTATO (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Florida District Office (FLA-DO) |
| 2/27/2012 | 25JFC12SWEET POTATO (ROOT & TUBER VEGETABLE) | 241PESTICIDE | Florida District Office (FLA-DO) |
| 7/7/2011 | 38CFT99DRIED SOUP, N.E.C. | 482NUTRIT LBL | Florida District Office (FLA-DO) |
| 7/7/2011 | 38CFT99DRIED SOUP, N.E.C. | Florida District Office (FLA-DO) | |
| 7/7/2011 | 38CFT99DRIED SOUP, N.E.C. | Florida District Office (FLA-DO) | |
| 9/3/2009 | 24FFB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | Florida District Office (FLA-DO) | |
| 4/30/2007 | 37JCE02BARBECUE SAUCE | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is PLG EXPORT IMPORT's FDA import refusal history?
PLG EXPORT IMPORT (FEI: 3012753870) has 9 FDA import refusal record(s) in our database, spanning from 4/30/2007 to 10/7/2016.
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. PLG EXPORT IMPORT's FEI number is 3012753870.
What types of violations has PLG EXPORT IMPORT received?
PLG EXPORT IMPORT has been cited for 13 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 PLG EXPORT IMPORT come from?
All FDA import refusal data for PLG EXPORT IMPORT 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.